Canonical Allele Identifier: CA645611453
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 693835
ClinVar RCV Id: RCV000855235
dbSNP Id: rs1603225114
COSMIC: COSM6188314 COSM6188315
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15159T>C , J01415.2:m.15159T>C GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.413T>C ENSP00000354554.2:p.Ile138Thr
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Search 100 bp 3'