Allele Registry

Canonical Allele Identifier: CA337100106

Gene: MT-ND6 HGNC NCBI

Linked Data - Variant Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.14582A>G

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000855131

ClinVar Variation:

693744

dbSNP:

41354845

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14582A>G , J01415.2:m.14582A>G	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361681.2:c.92T>C	ENSP00000354665.2:p.Val31Ala

Search 100 bp 5'

Search 100 bp 3'