Linked Data
ClinVar Variation Id:
752210
ClinVar RCV Id:
RCV000929334
dbSNP Id:
rs773247144
MyVariant Identifiers:
chrY:g.2655306T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.2787265T>C , CM000686.2:g.2787265T>C | GRCh38 |
| NC_000024.9:g.2655306T>C , CM000686.1:g.2655306T>C | GRCh37 |
| NC_000024.8:g.2715306T>C | NCBI36 |
| NG_011751.1:g.5487A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000679518.1:n.106+12526T>C | ||
| ENST00000679825.1:n.377T>C | ||
| ENST00000680285.1:n.320-2484T>C | ||
| ENST00000680845.1:n.165+212T>C | ||
| ENST00000681787.1:n.106+12526T>C | ||
| ENST00000681940.1:n.106+12526T>C | ||
| ENST00000383070.2:c.339A>G MANE Select | ENSP00000372547.1:p.Ala113= | |
| ENST00000383070.1:c.339A>G | ENSP00000372547.1:p.Ala113= | |
| NM_003140.2:c.339A>G | NP_003131.1:p.Ala113= | |
| NM_003140.3:c.339A>G MANE Select | NP_003131.1:p.Ala113= |