Canonical Allele Identifier: CA16603297
Gene: MT-CYB HGNC NCBI

Linked Data

ClinVar Variation Id: 377195
ClinVar RCV Id: RCV000440780 RCV000855370
dbSNP Id: rs879182710
MyVariant Identifiers: chrMT:g.15777G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.15777G>A , J01415.2:m.15777G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361789.2:c.1031G>A ENSP00000354554.2:p.Ser344Asn
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