Canonical Allele Identifier: CA414823271
Gene: MT-ND6 HGNC NCBI

Linked Data

MyVariant Identifiers: chrMT:g.14612G>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14612G>T , J01415.2:m.14612G>T GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361681.2:c.62C>A ENSP00000354665.2:p.Ser21Tyr