Canonical Allele Identifier: CA519593439
Gene:

Linked Data

MyVariant Identifiers: chrY:g.8775137C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8907096C>G , CM000686.2:g.8907096C>G GRCh38
NC_000024.9:g.8775137C>G , CM000686.1:g.8775137C>G GRCh37
NC_000024.8:g.8835137C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455422.5:n.112C>G