Canonical Allele Identifier: CA890190024
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs1438512275
MyVariant Identifiers: chr1:g.161184508A>C (hg19) chr1:g.161214718A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214718A>C , CM000663.2:g.161214718A>C GRCh38
NC_000001.10:g.161184508A>C , CM000663.1:g.161184508A>C GRCh37
NC_000001.9:g.159451132A>C NCBI36
NG_013352.1:g.20404A>C
NG_029043.1:g.4422A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4777A>C
ENST00000678492.1:n.4541A>C
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