Canonical Allele Identifier: CA526875198
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs572016427
gnomAD v2: 1-161184480-G-A
gnomAD v3: 1-161214690-G-A
gnomAD v4: 1-161214690-G-A
MyVariant Identifiers: chr1:g.161184480G>A (hg19) chr1:g.161214690G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214690G>A , CM000663.2:g.161214690G>A GRCh38
NC_000001.10:g.161184480G>A , CM000663.1:g.161184480G>A GRCh37
NC_000001.9:g.159451104G>A NCBI36
NG_013352.1:g.20376G>A
NG_029043.1:g.4394G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4749G>A
ENST00000678492.1:n.4513G>A
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