Linked Data
dbSNP Id:
rs111569776
gnomAD v3:
Y-12846292-G-GT
gnomAD v4:
Y-12846292-G-GT
MyVariant Identifiers:
chrY:g.12846292_12846293insT (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000024.10:g.12846301dup , CM000686.2:g.12846301dup | GRCh38 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000651177.1:c.6569-32dup | ENSP00000498372.1:n.6569-32dup | |
| ENST00000338981.7:c.6569-32dup MANE Select | ENSP00000342812.3:n.6569-32dup | |
| ENST00000426564.6:n.6596-32dup | ||
| NM_004654.3:c.6569-32dup | NP_004645.2:n.6569-32dup | |
| XM_011531469.1:c.6569-32dup | XP_011529771.1:n.6569-32dup | |
| XM_011531470.1:c.6335-32dup | XP_011529772.1:n.6335-32dup | |
| XM_017030078.2:c.6584-32dup | XP_016885567.1:n.6584-32dup | |
| NM_004654.4:c.6569-32dup MANE Select | NP_004645.2:n.6569-32dup |