Linked Data
ClinVar Variation Id:
355818
dbSNP Id:
rs371245873
ExAC:
6:152477245 G / A
gnomAD v2:
6-152477245-G-A
gnomAD v3:
6-152156110-G-A
gnomAD v4:
6-152156110-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152156110G>A , CM000668.2:g.152156110G>A | GRCh38 |
| NC_000006.11:g.152477245G>A , CM000668.1:g.152477245G>A | GRCh37 |
| NC_000006.10:g.152518938G>A | NCBI36 |
| NG_012855.1:g.486290C>T | |
| NG_012855.2:g.486290C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000354674.5:c.256-13C>T MANE Plus Clinical | ENSP00000346701.4:n.256-13C>T | |
| ENST00000367255.10:c.23791-13C>T MANE Select | ENSP00000356224.5:n.23791-13C>T | |
| ENST00000423061.6:c.23578-13C>T | ENSP00000396024.1:n.23578-13C>T | |
| ENST00000341594.9:c.22576-13C>T | ENSP00000341887.6:n.22576-13C>T | |
| ENST00000347037.9:n.470-13C>T | ||
| ENST00000354674.4:c.256-13C>T | ENSP00000346701.4:n.256-13C>T | |
| ENST00000367251.7:c.2557-13C>T | ENSP00000356220.3:n.2557-13C>T | |
| ENST00000367255.9:c.23791-13C>T | ENSP00000356224.5:n.23791-13C>T | |
| ENST00000367256.9:n.7483-13C>T | ||
| ENST00000367257.8:c.1729-13C>T | ENSP00000356226.4:n.1729-13C>T | |
| ENST00000409694.6:n.7375-13C>T | ||
| ENST00000423061.5:c.23578-13C>T | ENSP00000396024.1:n.23578-13C>T | |
| ENST00000460912.6:n.336-13C>T | ||
| ENST00000536990.5:n.628-13C>T | ||
| ENST00000539504.5:c.256-13C>T | ENSP00000441052.1:n.256-13C>T | |
| NM_033071.3:c.23578-13C>T | NP_149062.1:n.23578-13C>T | |
| NM_182961.3:c.23791-13C>T | NP_892006.3:n.23791-13C>T | |
| XM_006715407.1:c.23827-13C>T | XP_006715470.1:n.23827-13C>T | |
| XM_006715408.1:c.23815-13C>T | XP_006715471.1:n.23815-13C>T | |
| XM_006715409.1:c.23806-13C>T | XP_006715472.1:n.23806-13C>T | |
| XM_006715410.1:c.23827-13C>T | XP_006715473.1:n.23827-13C>T | |
| XM_006715411.1:c.23776-13C>T | XP_006715474.1:n.23776-13C>T | |
| XM_006715412.1:c.23812-13C>T | XP_006715475.1:n.23812-13C>T | |
| XM_006715413.1:c.23827-13C>T | XP_006715476.1:n.23827-13C>T | |
| XM_006715414.1:c.23755-13C>T | XP_006715477.1:n.23755-13C>T | |
| XM_006715415.1:c.23827-13C>T | XP_006715478.1:n.23827-13C>T | |
| XM_006715416.1:c.23812-13C>T | XP_006715479.1:n.23812-13C>T | |
| XM_006715417.1:c.23686-13C>T | XP_006715480.1:n.23686-13C>T | |
| XM_006715420.1:c.23674-13C>T | XP_006715483.1:n.23674-13C>T | |
| XM_006715421.1:c.23671-13C>T | XP_006715484.1:n.23671-13C>T | |
| XM_006715422.1:c.23668-13C>T | XP_006715485.1:n.23668-13C>T | |
| XM_006715423.1:c.23827-13C>T | XP_006715486.1:n.23827-13C>T | |
| XM_006715424.1:c.23827-13C>T | XP_006715487.1:n.23827-13C>T | |
| XM_006715425.1:c.23827-13C>T | XP_006715488.1:n.23827-13C>T | |
| XM_011535641.1:c.23824-13C>T | XP_011533943.1:n.23824-13C>T | |
| XM_011535642.1:c.23812-13C>T | XP_011533944.1:n.23812-13C>T | |
| XM_011535643.1:c.23662-13C>T | XP_011533945.1:n.23662-13C>T | |
| XM_011535644.1:c.22102-13C>T | XP_011533946.1:n.22102-13C>T | |
| XM_011535645.1:c.21595-13C>T | XP_011533947.1:n.21595-13C>T | |
| XM_011535647.1:c.17062-13C>T | XP_011533949.1:n.17062-13C>T | |
| NM_001347701.1:c.397-13C>T | NP_001334630.1:n.397-13C>T | |
| NM_001347702.1:c.256-13C>T | NP_001334631.1:n.256-13C>T | |
| XM_006715408.2:c.23815-13C>T | XP_006715471.1:n.23815-13C>T | |
| XM_006715410.2:c.23827-13C>T | XP_006715473.1:n.23827-13C>T | |
| XM_006715412.2:c.23812-13C>T | XP_006715475.1:n.23812-13C>T | |
| XM_006715413.2:c.23827-13C>T | XP_006715476.1:n.23827-13C>T | |
| XM_006715415.2:c.23827-13C>T | XP_006715478.1:n.23827-13C>T | |
| XM_006715416.2:c.23812-13C>T | XP_006715479.1:n.23812-13C>T | |
| XM_006715417.2:c.23686-13C>T | XP_006715480.1:n.23686-13C>T | |
| XM_006715420.2:c.23674-13C>T | XP_006715483.1:n.23674-13C>T | |
| XM_006715421.2:c.23671-13C>T | XP_006715484.1:n.23671-13C>T | |
| XM_006715423.2:c.23827-13C>T | XP_006715486.1:n.23827-13C>T | |
| XM_006715424.2:c.23827-13C>T | XP_006715487.1:n.23827-13C>T | |
| XM_006715425.2:c.23827-13C>T | XP_006715488.1:n.23827-13C>T | |
| XM_011535641.2:c.23824-13C>T | XP_011533943.1:n.23824-13C>T | |
| XM_011535642.2:c.23812-13C>T | XP_011533944.1:n.23812-13C>T | |
| XM_011535645.2:c.21595-13C>T | XP_011533947.1:n.21595-13C>T | |
| XM_017010608.1:c.23827-13C>T | XP_016866097.1:n.23827-13C>T | |
| XM_017010609.1:c.23827-13C>T | XP_016866098.1:n.23827-13C>T | |
| XM_017010610.1:c.23806-13C>T | XP_016866099.1:n.23806-13C>T | |
| XM_017010611.2:c.23800-13C>T | XP_016866100.1:n.23800-13C>T | |
| XM_017010612.1:c.23749-13C>T | XP_016866101.1:n.23749-13C>T | |
| XM_017010613.1:c.23824-13C>T | XP_016866102.1:n.23824-13C>T | |
| XM_017010614.1:c.23671-13C>T | XP_016866103.1:n.23671-13C>T | |
| XM_017010615.1:c.23671-13C>T | XP_016866104.1:n.23671-13C>T | |
| XM_017010616.1:c.23827-13C>T | XP_016866105.1:n.23827-13C>T | |
| XM_017010617.1:c.23824-13C>T | XP_016866106.1:n.23824-13C>T | |
| XM_017010618.1:c.23812-13C>T | XP_016866107.1:n.23812-13C>T | |
| XM_017010619.1:c.22102-13C>T | XP_016866108.1:n.22102-13C>T | |
| NM_182961.4:c.23791-13C>T MANE Select | NP_892006.3:n.23791-13C>T | |
| NM_001347701.2:c.397-13C>T | NP_001334630.1:n.397-13C>T | |
| NM_001347702.2:c.256-13C>T MANE Plus Clinical | NP_001334631.1:n.256-13C>T | |
| NM_033071.5:c.23578-13C>T | NP_149062.2:n.23578-13C>T |