Linked Data
MyVariant Identifiers:
chrY:g.2734884T>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.2866843T>A , CM000686.2:g.2866843T>A | GRCh38 |
| NC_000024.9:g.2734884T>A , CM000686.1:g.2734884T>A | GRCh37 |
| NC_000024.8:g.2794884T>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000250784.13:c.741T>A MANE Select | ENSP00000250784.7:p.Thr247= | |
| ENST00000250784.12:c.741T>A | ENSP00000250784.7:p.Thr247= | |
| ENST00000430575.1:c.768T>A | ENSP00000415317.1:p.Thr256= | |
| ENST00000477725.1:n.885T>A | ||
| ENST00000515575.1:n.42+12072T>A | ||
| NM_001008.3:c.741T>A | NP_000999.1:p.Thr247= | |
| NM_001008.4:c.741T>A MANE Select | NP_000999.1:p.Thr247= |