Canonical Allele Identifier: CA337098956
Gene: MT-ND4L HGNC NCBI
dbSNP:
2853488
MyVariant.info:
GRCh38 chrMT:g.10688G>A
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.10688G>A , J01415.2:m.10688G>A GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361335.1:c.219G>A ENSP00000354728.1:p.Val73=
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