Canonical Allele Identifier: CA519593489
Gene:

Linked Data

MyVariant Identifiers: chrY:g.8775153G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8907112G>C , CM000686.2:g.8907112G>C GRCh38
NC_000024.9:g.8775153G>C , CM000686.1:g.8775153G>C GRCh37
NC_000024.8:g.8835153G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000455422.5:n.128G>C