Canonical Allele Identifier: CA519593508
Gene:

Linked Data

MyVariant Identifiers: chrY:g.8775160C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8907119C>A , CM000686.2:g.8907119C>A GRCh38
NC_000024.9:g.8775160C>A , CM000686.1:g.8775160C>A GRCh37
NC_000024.8:g.8835160C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455422.5:n.135C>A