Canonical Allele Identifier: CA519593485
Gene:

Linked Data

MyVariant Identifiers: chrY:g.8775152T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8907111T>A , CM000686.2:g.8907111T>A GRCh38
NC_000024.9:g.8775152T>A , CM000686.1:g.8775152T>A GRCh37
NC_000024.8:g.8835152T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000455422.5:n.127T>A