Canonical Allele Identifier: CA414772567
Gene: MT-ND1 HGNC NCBI

Linked Data

dbSNP Id: rs1556422709
MyVariant Identifiers: chrMT:g.3337G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3337G>C , J01415.2:m.3337G>C GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.31G>C ENSP00000354687.2:p.Val11Leu
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