Linked Data
ClinVar Variation Id:
1793749
ClinVar RCV Id:
RCV002426312
MyVariant Identifiers:
chr15:g.73615827A>G (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73323486A>G , CM000677.2:g.73323486A>G | GRCh38 |
| NC_000015.9:g.73615827A>G , CM000677.1:g.73615827A>G | GRCh37 |
| NC_000015.8:g.71402880A>G | NCBI36 |
| NG_009063.1:g.50779T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.2607T>C MANE Select | ENSP00000261917.3:p.Ala869= | |
| ENST00000261917.3:c.2607T>C | ENSP00000261917.3:p.Ala869= | |
| NM_005477.2:c.2607T>C | NP_005468.1:p.Ala869= | |
| XM_011521148.1:c.1389T>C | XP_011519450.1:p.Ala463= | |
| XM_011521148.2:c.1389T>C | XP_011519450.1:p.Ala463= | |
| NM_005477.3:c.2607T>C MANE Select | NP_005468.1:p.Ala869= |