Canonical Allele Identifier: CA519539096
Gene:

Linked Data

MyVariant Identifiers: chrY:g.7548830G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7680789G>T , CM000686.2:g.7680789G>T GRCh38
NC_000024.9:g.7548830G>T , CM000686.1:g.7548830G>T GRCh37
NC_000024.8:g.7608830G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439805.1:n.541G>T