Canonical Allele Identifier: CA519593631
Gene:

Linked Data

MyVariant Identifiers: chrY:g.8775201C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8907160C>G , CM000686.2:g.8907160C>G GRCh38
NC_000024.9:g.8775201C>G , CM000686.1:g.8775201C>G GRCh37
NC_000024.8:g.8835201C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000455422.5:n.176C>G