Canonical Allele Identifier: CA519539068
Gene:

Linked Data

MyVariant Identifiers: chrY:g.7548828A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.7680787A>C , CM000686.2:g.7680787A>C GRCh38
NC_000024.9:g.7548828A>C , CM000686.1:g.7548828A>C GRCh37
NC_000024.8:g.7608828A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000439805.1:n.539A>C