Canonical Allele Identifier: CA519539058
Gene:

Linked Data

MyVariant Identifiers: chrY:g.7548827T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7680786T>C , CM000686.2:g.7680786T>C GRCh38
NC_000024.9:g.7548827T>C , CM000686.1:g.7548827T>C GRCh37
NC_000024.8:g.7608827T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439805.1:n.538T>C