Linked Data
ClinVar Variation Id:
1156028
dbSNP Id:
rs557593730
ExAC:
8:145639727 G / A
gnomAD v2:
8-145639727-G-A
gnomAD v3:
8-144414343-G-A
gnomAD v4:
8-144414343-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.144414343G>A , CM000670.2:g.144414343G>A | GRCh38 |
| NC_000008.10:g.145639727G>A , CM000670.1:g.145639727G>A | GRCh37 |
| NC_000008.9:g.145610535G>A | NCBI36 |
| NG_012234.2:g.7548C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301305.8:c.1068C>T MANE Select | ENSP00000301305.4:p.Val356= | |
| ENST00000276833.9:c.993C>T | ENSP00000276833.5:p.Val331= | |
| ENST00000301305.7:c.1068C>T | ENSP00000301305.3:p.Val356= | |
| NM_017767.2:c.993C>T | NP_060237.2:p.Val331= | |
| NM_130849.3:c.1068C>T | NP_570901.2:p.Val356= | |
| XM_006716599.1:c.1068C>T | XP_006716662.1:p.Val356= | |
| XM_011517153.1:c.786C>T | XP_011515455.1:p.Val262= | |
| XM_024447188.1:c.786C>T | XP_024302956.1:p.Val262= | |
| XM_024447189.1:c.786C>T | XP_024302957.1:p.Val262= | |
| NM_001374839.1:c.786C>T | NP_001361768.1:p.Val262= | |
| NM_017767.3:c.993C>T | NP_060237.3:p.Val331= | |
| NM_130849.4:c.1068C>T MANE Select | NP_570901.3:p.Val356= |