Canonical Allele Identifier: CA519593572
Gene:

Linked Data

MyVariant Identifiers: chrY:g.8775181C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8907140C>G , CM000686.2:g.8907140C>G GRCh38
NC_000024.9:g.8775181C>G , CM000686.1:g.8775181C>G GRCh37
NC_000024.8:g.8835181C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455422.5:n.156C>G