Canonical Allele Identifier: CA519538960
Gene:

Linked Data

MyVariant Identifiers: chrY:g.7548821C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7680780C>A , CM000686.2:g.7680780C>A GRCh38
NC_000024.9:g.7548821C>A , CM000686.1:g.7548821C>A GRCh37
NC_000024.8:g.7608821C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439805.1:n.532C>A