Linked Data
ClinVar Variation Id:
13313
ClinVar RCV Id:
RCV002468931
dbSNP Id:
rs121918485
ExAC:
11:46749689 G / A
gnomAD v2:
11-46749689-G-A
gnomAD v4:
11-46728139-G-A
COSMIC:
COSM4033078
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.46728139G>A , CM000673.2:g.46728139G>A | GRCh38 |
| NC_000011.9:g.46749689G>A , CM000673.1:g.46749689G>A | GRCh37 |
| NC_000011.8:g.46706265G>A | NCBI36 |
| NG_008953.1:g.13947G>A , LRG_551:g.13947G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000311907.10:c.1274G>A MANE Select | ENSP00000308541.5:p.Arg425His | |
| ENST00000311907.9:c.1274G>A | ENSP00000308541.5:p.Arg425His | |
| ENST00000530231.5:c.1274G>A | ENSP00000433907.1:p.Arg425His | |
| NM_000506.3:c.1274G>A | NP_000497.1:p.Arg425His | |
| NM_000506.4:c.1274G>A , LRG_551t1:c.1274G>A | NP_000497.1:p.Arg425His | |
| NM_001311257.1:c.1226G>A | NP_001298186.1:p.Arg409His | |
| XR_428840.2:n.1318G>A | ||
| XR_428840.4:n.1309G>A | ||
| NM_000506.5:c.1274G>A MANE Select | NP_000497.1:p.Arg425His | |
| NM_001311257.2:c.1226G>A | NP_001298186.1:p.Arg409His |