Linked Data
ClinVar Variation Id:
2918486
ClinVar RCV Id:
RCV003615501
dbSNP Id:
rs1567766661
gnomAD v2:
15-73614998-G-A
gnomAD v3:
15-73322657-G-A
gnomAD v4:
15-73322657-G-A
COSMIC:
COSM3722008
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73322657G>A , CM000677.2:g.73322657G>A | GRCh38 |
| NC_000015.9:g.73614998G>A , CM000677.1:g.73614998G>A | GRCh37 |
| NC_000015.8:g.71402051G>A | NCBI36 |
| NG_009063.1:g.51608C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.3436C>T MANE Select | ENSP00000261917.3:p.Pro1146Ser | |
| ENST00000261917.3:c.3436C>T | ENSP00000261917.3:p.Pro1146Ser | |
| NM_005477.2:c.3436C>T | NP_005468.1:p.Pro1146Ser | |
| XM_011521148.1:c.2218C>T | XP_011519450.1:p.Pro740Ser | |
| XM_011521148.2:c.2218C>T | XP_011519450.1:p.Pro740Ser | |
| NM_005477.3:c.3436C>T MANE Select | NP_005468.1:p.Pro1146Ser |