Canonical Allele Identifier: CA519539005
Gene:

Linked Data

MyVariant Identifiers: chrY:g.7548824C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7680783C>G , CM000686.2:g.7680783C>G GRCh38
NC_000024.9:g.7548824C>G , CM000686.1:g.7548824C>G GRCh37
NC_000024.8:g.7608824C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439805.1:n.535C>G