Canonical Allele Identifier: CA16603354
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 377369
ClinVar RCV Id: RCV000426856 RCV000855387 RCV003319197
dbSNP Id: rs1057520206
MyVariant Identifiers: chrMT:g.15848A>G (hg38)
ERepo: CA16603354/MONDO:0044970/014
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15848A>G , J01415.2:m.15848A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.1102A>G ENSP00000354554.2:p.Thr368Ala
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