Allele Registry

Canonical Allele Identifier: CA345757

Gene: MT-CYB HGNC NCBI

Linked Data - Predicted Effect Evidence

MyVariant.info:

GRCh38 chrMT:g.14905G>A

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000133450

ClinVar Variation:

143919

dbSNP:

193302983

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14905G>A , J01415.2:m.14905G>A	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361789.2:c.159G>A	ENSP00000354554.2:p.Met53Ile

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