Canonical Allele Identifier: CA337099036
Gene: MT-ND4 HGNC NCBI
dbSNP:
2857284
MyVariant.info:
GRCh38 chrMT:g.10873T>C
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10873T>C , J01415.2:m.10873T>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361381.2:c.114T>C ENSP00000354961.2:p.Pro38=
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