Linked Data
ClinVar Variation Id:
379571
dbSNP Id:
rs910956017
gnomAD v2:
6-152590313-G-A
gnomAD v3:
6-152269178-G-A
gnomAD v4:
6-152269178-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.152269178G>A , CM000668.2:g.152269178G>A | GRCh38 |
| NC_000006.11:g.152590313G>A , CM000668.1:g.152590313G>A | GRCh37 |
| NC_000006.10:g.152632006G>A | NCBI36 |
| NG_012855.1:g.373222C>T | |
| NG_012855.2:g.373222C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000367255.10:c.18682C>T MANE Select | ENSP00000356224.5:p.Gln6228Ter | |
| ENST00000423061.6:c.18469C>T | ENSP00000396024.1:p.Gln6157Ter | |
| ENST00000341594.9:c.17467C>T | ENSP00000341887.6:p.Gln5823Ter | |
| ENST00000367255.9:c.18682C>T | ENSP00000356224.5:p.Gln6228Ter | |
| ENST00000367256.9:n.2374C>T | ||
| ENST00000409694.6:n.2266C>T | ||
| ENST00000423061.5:c.18469C>T | ENSP00000396024.1:p.Gln6157Ter | |
| NM_033071.3:c.18469C>T | NP_149062.1:p.Gln6157Ter | |
| NM_182961.3:c.18682C>T | NP_892006.3:p.Gln6228Ter | |
| XM_006715407.1:c.18718C>T | XP_006715470.1:p.Gln6240Ter | |
| XM_006715408.1:c.18706C>T | XP_006715471.1:p.Gln6236Ter | |
| XM_006715409.1:c.18697C>T | XP_006715472.1:p.Gln6233Ter | |
| XM_006715410.1:c.18718C>T | XP_006715473.1:p.Gln6240Ter | |
| XM_006715411.1:c.18667C>T | XP_006715474.1:p.Gln6223Ter | |
| XM_006715412.1:c.18703C>T | XP_006715475.1:p.Gln6235Ter | |
| XM_006715413.1:c.18718C>T | XP_006715476.1:p.Gln6240Ter | |
| XM_006715414.1:c.18646C>T | XP_006715477.1:p.Gln6216Ter | |
| XM_006715415.1:c.18718C>T | XP_006715478.1:p.Gln6240Ter | |
| XM_006715416.1:c.18703C>T | XP_006715479.1:p.Gln6235Ter | |
| XM_006715417.1:c.18577C>T | XP_006715480.1:p.Gln6193Ter | |
| XM_006715420.1:c.18565C>T | XP_006715483.1:p.Gln6189Ter | |
| XM_006715421.1:c.18562C>T | XP_006715484.1:p.Gln6188Ter | |
| XM_006715422.1:c.18559C>T | XP_006715485.1:p.Gln6187Ter | |
| XM_006715423.1:c.18718C>T | XP_006715486.1:p.Gln6240Ter | |
| XM_006715424.1:c.18718C>T | XP_006715487.1:p.Gln6240Ter | |
| XM_006715425.1:c.18718C>T | XP_006715488.1:p.Gln6240Ter | |
| XM_011535641.1:c.18715C>T | XP_011533943.1:p.Gln6239Ter | |
| XM_011535642.1:c.18703C>T | XP_011533944.1:p.Gln6235Ter | |
| XM_011535643.1:c.18553C>T | XP_011533945.1:p.Gln6185Ter | |
| XM_011535644.1:c.16993C>T | XP_011533946.1:p.Gln5665Ter | |
| XM_011535645.1:c.16486C>T | XP_011533947.1:p.Gln5496Ter | |
| XM_011535646.1:c.18718C>T | XP_011533948.1:p.Gln6240Ter | |
| XM_011535647.1:c.11953C>T | XP_011533949.1:p.Gln3985Ter | |
| XM_006715408.2:c.18706C>T | XP_006715471.1:p.Gln6236Ter | |
| XM_006715410.2:c.18718C>T | XP_006715473.1:p.Gln6240Ter | |
| XM_006715412.2:c.18703C>T | XP_006715475.1:p.Gln6235Ter | |
| XM_006715413.2:c.18718C>T | XP_006715476.1:p.Gln6240Ter | |
| XM_006715415.2:c.18718C>T | XP_006715478.1:p.Gln6240Ter | |
| XM_006715416.2:c.18703C>T | XP_006715479.1:p.Gln6235Ter | |
| XM_006715417.2:c.18577C>T | XP_006715480.1:p.Gln6193Ter | |
| XM_006715420.2:c.18565C>T | XP_006715483.1:p.Gln6189Ter | |
| XM_006715421.2:c.18562C>T | XP_006715484.1:p.Gln6188Ter | |
| XM_006715423.2:c.18718C>T | XP_006715486.1:p.Gln6240Ter | |
| XM_006715424.2:c.18718C>T | XP_006715487.1:p.Gln6240Ter | |
| XM_006715425.2:c.18718C>T | XP_006715488.1:p.Gln6240Ter | |
| XM_011535641.2:c.18715C>T | XP_011533943.1:p.Gln6239Ter | |
| XM_011535642.2:c.18703C>T | XP_011533944.1:p.Gln6235Ter | |
| XM_011535645.2:c.16486C>T | XP_011533947.1:p.Gln5496Ter | |
| XM_017010608.1:c.18718C>T | XP_016866097.1:p.Gln6240Ter | |
| XM_017010609.1:c.18718C>T | XP_016866098.1:p.Gln6240Ter | |
| XM_017010610.1:c.18697C>T | XP_016866099.1:p.Gln6233Ter | |
| XM_017010611.2:c.18691C>T | XP_016866100.1:p.Gln6231Ter | |
| XM_017010612.1:c.18640C>T | XP_016866101.1:p.Gln6214Ter | |
| XM_017010613.1:c.18715C>T | XP_016866102.1:p.Gln6239Ter | |
| XM_017010614.1:c.18562C>T | XP_016866103.1:p.Gln6188Ter | |
| XM_017010615.1:c.18562C>T | XP_016866104.1:p.Gln6188Ter | |
| XM_017010616.1:c.18718C>T | XP_016866105.1:p.Gln6240Ter | |
| XM_017010617.1:c.18715C>T | XP_016866106.1:p.Gln6239Ter | |
| XM_017010618.1:c.18703C>T | XP_016866107.1:p.Gln6235Ter | |
| XM_017010619.1:c.16993C>T | XP_016866108.1:p.Gln5665Ter | |
| XR_001743287.1:n.19201C>T | ||
| NM_182961.4:c.18682C>T MANE Select | NP_892006.3:p.Gln6228Ter | |
| NM_033071.5:c.18469C>T | NP_149062.2:p.Gln6157Ter |