Linked Data
ClinVar Variation Id:
1305239
ClinVar RCV Id:
RCV001768446
dbSNP Id:
rs144261466
ExAC:
1:27429001 G / A
gnomAD v2:
1-27429001-G-A
gnomAD v3:
1-27102510-G-A
gnomAD v4:
1-27102510-G-A
COSMIC:
COSM907818
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.27102510G>A , CM000663.2:g.27102510G>A | GRCh38 |
| NC_000001.10:g.27429001G>A , CM000663.1:g.27429001G>A | GRCh37 |
| NC_000001.9:g.27301588G>A | NCBI36 |
| NG_030006.1:g.57451C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000263980.8:c.1695C>T MANE Select | ENSP00000263980.3:p.Gly565= | |
| ENST00000263980.7:c.1695C>T | ENSP00000263980.3:p.Gly565= | |
| ENST00000374089.5:n.920C>T | ||
| ENST00000447808.1:n.172C>T | ||
| NM_003047.4:c.1695C>T | NP_003038.2:p.Gly565= | |
| NR_046474.1:n.2030C>T | ||
| XM_011542021.1:c.1365C>T | XP_011540323.1:p.Gly455= | |
| XM_011542021.3:c.1365C>T | XP_011540323.1:p.Gly455= | |
| NM_003047.5:c.1695C>T MANE Select | NP_003038.2:p.Gly565= | |
| NR_046474.2:n.2025C>T |