Linked Data
ClinVar Variation Id:
1602544
ClinVar RCV Id:
RCV002141462
dbSNP Id:
rs1343121998
gnomAD v4:
10-119651831-G-A
MyVariant Identifiers:
chr10:g.121411343G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.119651831G>A , CM000672.2:g.119651831G>A | GRCh38 |
| NC_000010.10:g.121411343G>A , CM000672.1:g.121411343G>A | GRCh37 |
| NC_000010.9:g.121401333G>A | NCBI36 |
| NG_016125.1:g.5462G>A , LRG_742:g.5462G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369085.8:c.156G>A MANE Select | ENSP00000358081.4:p.Pro52= | |
| ENST00000369085.7:c.156G>A | ENSP00000358081.3:p.Pro52= | |
| NM_004281.3:c.156G>A , LRG_742t1:c.156G>A | NP_004272.2:p.Pro52= | |
| XM_005270287.1:c.156G>A | XP_005270344.1:p.Pro52= | |
| XM_005270287.2:c.156G>A | XP_005270344.1:p.Pro52= | |
| NM_004281.4:c.156G>A MANE Select | NP_004272.2:p.Pro52= |