Canonical Allele Identifier: CA1202648727
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665964541
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214688G>A , CM000663.2:g.161214688G>A GRCh38
NC_000001.10:g.161184478G>A , CM000663.1:g.161184478G>A GRCh37
NC_000001.9:g.159451102G>A NCBI36
NG_013352.1:g.20374G>A
NG_029043.1:g.4392G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4747G>A
ENST00000678492.1:n.4511G>A
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