Linked Data
ClinVar Variation Id:
2626611
ClinVar RCV Id:
RCV003384151
gnomAD v4:
15-73367860-C-A
MyVariant Identifiers:
chr15:g.73660201C>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73367860C>A , CM000677.2:g.73367860C>A | GRCh38 |
| NC_000015.9:g.73660201C>A , CM000677.1:g.73660201C>A | GRCh37 |
| NC_000015.8:g.71447254C>A | NCBI36 |
| NG_009063.1:g.6405G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.411G>T MANE Select | ENSP00000261917.3:p.Ala137= | |
| ENST00000261917.3:c.411G>T | ENSP00000261917.3:p.Ala137= | |
| NM_005477.2:c.411G>T | NP_005468.1:p.Ala137= | |
| NM_005477.3:c.411G>T MANE Select | NP_005468.1:p.Ala137= |