Canonical Allele Identifier: CA519593634
Gene:

Linked Data

MyVariant Identifiers: chrY:g.8775202A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8907161A>T , CM000686.2:g.8907161A>T GRCh38
NC_000024.9:g.8775202A>T , CM000686.1:g.8775202A>T GRCh37
NC_000024.8:g.8835202A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000455422.5:n.177A>T