Canonical Allele Identifier: CA519593511
Gene:

Linked Data

MyVariant Identifiers: chrY:g.8775161A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8907120A>C , CM000686.2:g.8907120A>C GRCh38
NC_000024.9:g.8775161A>C , CM000686.1:g.8775161A>C GRCh37
NC_000024.8:g.8835161A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000455422.5:n.136A>C