Canonical Allele Identifier: CA337100193
Gene: MT-CYB HGNC NCBI

Linked Data

dbSNP Id: rs878992560
MyVariant Identifiers: chrMT:g.14893A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.14893A>G , J01415.2:m.14893A>G GRCh38

Transcript Alleles

HGVS Amino-acid change
ENST00000361789.2:c.147A>G ENSP00000354554.2:p.Leu49=