Canonical Allele Identifier: CA519586498
Gene: MTND2P3 HGNC NCBI

Linked Data

MyVariant Identifiers: chrY:g.8240730A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000024.10:g.8372689A>C , CM000686.2:g.8372689A>C GRCh38
NC_000024.9:g.8240730A>C , CM000686.1:g.8240730A>C GRCh37
NC_000024.8:g.8300730A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000452458.1:n.449A>C