Canonical Allele Identifier: CA519593639
Gene:

Linked Data

MyVariant Identifiers: chrY:g.8775204A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8907163A>C , CM000686.2:g.8907163A>C GRCh38
NC_000024.9:g.8775204A>C , CM000686.1:g.8775204A>C GRCh37
NC_000024.8:g.8835204A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000455422.5:n.179A>C