Canonical Allele Identifier: CA337099756
Gene: MT-ND5 HGNC NCBI

Linked Data

dbSNP Id: rs376146541
MyVariant Identifiers: chrMT:g.13626C>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.13626C>T , J01415.2:m.13626C>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361567.2:c.1290C>T ENSP00000354813.2:p.Thr430=