Linked Data
ClinVar Variation Id:
284568
dbSNP Id:
rs141170182
ExAC:
6:152542605 G / A
gnomAD v2:
6-152542605-G-A
gnomAD v3:
6-152221470-G-A
gnomAD v4:
6-152221470-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152221470G>A , CM000668.2:g.152221470G>A | GRCh38 |
| NC_000006.11:g.152542605G>A , CM000668.1:g.152542605G>A | GRCh37 |
| NC_000006.10:g.152584298G>A | NCBI36 |
| NG_012855.1:g.420930C>T | |
| NG_012855.2:g.420930C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367255.10:c.21612C>T MANE Select | ENSP00000356224.5:p.Pro7204= | |
| ENST00000423061.6:c.21399C>T | ENSP00000396024.1:p.Pro7133= | |
| ENST00000341594.9:c.20397C>T | ENSP00000341887.6:p.Pro6799= | |
| ENST00000367251.7:c.378C>T | ENSP00000356220.3:p.Pro126= | |
| ENST00000367255.9:c.21612C>T | ENSP00000356224.5:p.Pro7204= | |
| ENST00000367256.9:n.5304C>T | ||
| ENST00000409694.6:n.5196C>T | ||
| ENST00000423061.5:c.21399C>T | ENSP00000396024.1:p.Pro7133= | |
| NM_033071.3:c.21399C>T | NP_149062.1:p.Pro7133= | |
| NM_182961.3:c.21612C>T | NP_892006.3:p.Pro7204= | |
| XM_006715407.1:c.21648C>T | XP_006715470.1:p.Pro7216= | |
| XM_006715408.1:c.21636C>T | XP_006715471.1:p.Pro7212= | |
| XM_006715409.1:c.21627C>T | XP_006715472.1:p.Pro7209= | |
| XM_006715410.1:c.21648C>T | XP_006715473.1:p.Pro7216= | |
| XM_006715411.1:c.21597C>T | XP_006715474.1:p.Pro7199= | |
| XM_006715412.1:c.21633C>T | XP_006715475.1:p.Pro7211= | |
| XM_006715413.1:c.21648C>T | XP_006715476.1:p.Pro7216= | |
| XM_006715414.1:c.21576C>T | XP_006715477.1:p.Pro7192= | |
| XM_006715415.1:c.21648C>T | XP_006715478.1:p.Pro7216= | |
| XM_006715416.1:c.21633C>T | XP_006715479.1:p.Pro7211= | |
| XM_006715417.1:c.21507C>T | XP_006715480.1:p.Pro7169= | |
| XM_006715420.1:c.21495C>T | XP_006715483.1:p.Pro7165= | |
| XM_006715421.1:c.21492C>T | XP_006715484.1:p.Pro7164= | |
| XM_006715422.1:c.21489C>T | XP_006715485.1:p.Pro7163= | |
| XM_006715423.1:c.21648C>T | XP_006715486.1:p.Pro7216= | |
| XM_006715424.1:c.21648C>T | XP_006715487.1:p.Pro7216= | |
| XM_006715425.1:c.21648C>T | XP_006715488.1:p.Pro7216= | |
| XM_011535641.1:c.21645C>T | XP_011533943.1:p.Pro7215= | |
| XM_011535642.1:c.21633C>T | XP_011533944.1:p.Pro7211= | |
| XM_011535643.1:c.21483C>T | XP_011533945.1:p.Pro7161= | |
| XM_011535644.1:c.19923C>T | XP_011533946.1:p.Pro6641= | |
| XM_011535645.1:c.19416C>T | XP_011533947.1:p.Pro6472= | |
| XM_011535647.1:c.14883C>T | XP_011533949.1:p.Pro4961= | |
| XM_006715408.2:c.21636C>T | XP_006715471.1:p.Pro7212= | |
| XM_006715410.2:c.21648C>T | XP_006715473.1:p.Pro7216= | |
| XM_006715412.2:c.21633C>T | XP_006715475.1:p.Pro7211= | |
| XM_006715413.2:c.21648C>T | XP_006715476.1:p.Pro7216= | |
| XM_006715415.2:c.21648C>T | XP_006715478.1:p.Pro7216= | |
| XM_006715416.2:c.21633C>T | XP_006715479.1:p.Pro7211= | |
| XM_006715417.2:c.21507C>T | XP_006715480.1:p.Pro7169= | |
| XM_006715420.2:c.21495C>T | XP_006715483.1:p.Pro7165= | |
| XM_006715421.2:c.21492C>T | XP_006715484.1:p.Pro7164= | |
| XM_006715423.2:c.21648C>T | XP_006715486.1:p.Pro7216= | |
| XM_006715424.2:c.21648C>T | XP_006715487.1:p.Pro7216= | |
| XM_006715425.2:c.21648C>T | XP_006715488.1:p.Pro7216= | |
| XM_011535641.2:c.21645C>T | XP_011533943.1:p.Pro7215= | |
| XM_011535642.2:c.21633C>T | XP_011533944.1:p.Pro7211= | |
| XM_011535645.2:c.19416C>T | XP_011533947.1:p.Pro6472= | |
| XM_017010608.1:c.21648C>T | XP_016866097.1:p.Pro7216= | |
| XM_017010609.1:c.21648C>T | XP_016866098.1:p.Pro7216= | |
| XM_017010610.1:c.21627C>T | XP_016866099.1:p.Pro7209= | |
| XM_017010611.2:c.21621C>T | XP_016866100.1:p.Pro7207= | |
| XM_017010612.1:c.21570C>T | XP_016866101.1:p.Pro7190= | |
| XM_017010613.1:c.21645C>T | XP_016866102.1:p.Pro7215= | |
| XM_017010614.1:c.21492C>T | XP_016866103.1:p.Pro7164= | |
| XM_017010615.1:c.21492C>T | XP_016866104.1:p.Pro7164= | |
| XM_017010616.1:c.21648C>T | XP_016866105.1:p.Pro7216= | |
| XM_017010617.1:c.21645C>T | XP_016866106.1:p.Pro7215= | |
| XM_017010618.1:c.21633C>T | XP_016866107.1:p.Pro7211= | |
| XM_017010619.1:c.19923C>T | XP_016866108.1:p.Pro6641= | |
| NM_182961.4:c.21612C>T MANE Select | NP_892006.3:p.Pro7204= | |
| NM_033071.5:c.21399C>T | NP_149062.2:p.Pro7133= |