Canonical Allele Identifier: CA519538651
Gene:

Linked Data

MyVariant Identifiers: chrY:g.7548801G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7680760G>A , CM000686.2:g.7680760G>A GRCh38
NC_000024.9:g.7548801G>A , CM000686.1:g.7548801G>A GRCh37
NC_000024.8:g.7608801G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000439805.1:n.512G>A