Linked Data
MyVariant Identifiers:
chrY:g.14969565A>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12857640A>T , CM000686.2:g.12857640A>T | GRCh38 |
| NC_000024.9:g.14969565A>T , CM000686.1:g.14969565A>T | GRCh37 |
| NC_000024.8:g.13478959A>T | NCBI36 |
| NG_008311.1:g.161406A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651177.1:c.7509A>T | ENSP00000498372.1:p.Ser2503= | |
| ENST00000338981.7:c.7509A>T MANE Select | ENSP00000342812.3:p.Ser2503= | |
| ENST00000426564.6:n.7536A>T | ||
| ENST00000453031.1:c.554A>T | ||
| ENST00000471409.1:n.828A>T | ||
| NM_004654.3:c.7509A>T | NP_004645.2:p.Ser2503= | |
| XM_011531469.1:c.7509A>T | XP_011529771.1:p.Ser2503= | |
| XM_011531470.1:c.7275A>T | XP_011529772.1:p.Ser2425= | |
| XM_017030078.2:c.7524A>T | XP_016885567.1:p.Ser2508= | |
| NM_004654.4:c.7509A>T MANE Select | NP_004645.2:p.Ser2503= |