Canonical Allele Identifier: CA519539095
Gene:

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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