Canonical Allele Identifier: CA519538990
Gene:

Linked Data

MyVariant Identifiers: chrY:g.7548823G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7680782G>C , CM000686.2:g.7680782G>C GRCh38
NC_000024.9:g.7548823G>C , CM000686.1:g.7548823G>C GRCh37
NC_000024.8:g.7608823G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439805.1:n.534G>C