Canonical Allele Identifier: CA414773957
Gene: MT-ND1 HGNC NCBI

Linked Data

ClinVar Variation Id: 618726
ClinVar RCV Id: RCV000757485
dbSNP Id: rs1569483910
MyVariant Identifiers: chrMT:g.3991A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.3991A>G , J01415.2:m.3991A>G GRCh38

Transcript Alleles

HGVS Amino-acid Change
ENST00000361390.2:c.685A>G ENSP00000354687.2:p.Thr229Ala
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