Canonical Allele Identifier: CA519593622
Gene:

Linked Data

MyVariant Identifiers: chrY:g.8775198C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8907157C>G , CM000686.2:g.8907157C>G GRCh38
NC_000024.9:g.8775198C>G , CM000686.1:g.8775198C>G GRCh37
NC_000024.8:g.8835198C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455422.5:n.173C>G