Canonical Allele Identifier: CA519593482
Gene:

Linked Data

MyVariant Identifiers: chrY:g.8775151T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8907110T>C , CM000686.2:g.8907110T>C GRCh38
NC_000024.9:g.8775151T>C , CM000686.1:g.8775151T>C GRCh37
NC_000024.8:g.8835151T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455422.5:n.126T>C