Canonical Allele Identifier: CA16043602

Gene: MT-ND6

Linked Data

• ClinVar Variation Id: 374080
• ClinVar RCV Id: RCV000415203 ; RCV000855133
• dbSNP Id: rs1057518882
• MyVariant Identifiers: chrMT:g.14598T>C (hg38)
• ERepo: CA16043602/MONDO:0044970/014

Genomic Alleles

HGVS	Genome Assembly
NC_012920.1:m.14598T>C , J01415.2:m.14598T>C	GRCh38

Transcript Alleles

HGVS	Amino-acid Change
ENST00000361681.2:c.76A>G	ENSP00000354665.2:p.Ile26Val