Canonical Allele Identifier: CA31677466
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs976950142
gnomAD v3: 1-161214681-G-A
gnomAD v4: 1-161214681-G-A
MyVariant Identifiers: chr1:g.161184471G>A (hg19) chr1:g.161214681G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214681G>A , CM000663.2:g.161214681G>A GRCh38
NC_000001.10:g.161184471G>A , CM000663.1:g.161184471G>A GRCh37
NC_000001.9:g.159451095G>A NCBI36
NG_013352.1:g.20367G>A
NG_029043.1:g.4385G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4740G>A
ENST00000678492.1:n.4504G>A
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