Canonical Allele Identifier: CA890190025
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs1438512275
gnomAD v3: 1-161214718-A-G
gnomAD v4: 1-161214718-A-G
MyVariant Identifiers: chr1:g.161184508A>G (hg19) chr1:g.161214718A>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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