Canonical Allele Identifier: CA519586541
Gene: MTND2P3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.8240739G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8372698G>A , CM000686.2:g.8372698G>A GRCh38
NC_000024.9:g.8240739G>A , CM000686.1:g.8240739G>A GRCh37
NC_000024.8:g.8300739G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000452458.1:n.458G>A