Canonical Allele Identifier: CA345758
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 143924
ClinVar RCV Id: RCV000133455 RCV000855290
dbSNP Id: rs193302993
MyVariant Identifiers: chrMT:g.15431G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15431G>A , J01415.2:m.15431G>A GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.685G>A ENSP00000354554.2:p.Ala229Thr
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