Canonical Allele Identifier: CA269989
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 140592
ClinVar RCV Id: RCV000128807 RCV000855273 RCV002221492
dbSNP Id: rs2853508
MyVariant Identifiers: chrMT:g.15326A>G (hg38)
ERepo: CA269989/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15326A>G , J01415.2:m.15326A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.580A>G ENSP00000354554.2:p.Thr194Ala
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