Canonical Allele Identifier: CA1202648735
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665966418
gnomAD v3: 1-161214703-C-T
gnomAD v4: 1-161214703-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214703C>T , CM000663.2:g.161214703C>T GRCh38
NC_000001.10:g.161184493C>T , CM000663.1:g.161184493C>T GRCh37
NC_000001.9:g.159451117C>T NCBI36
NG_013352.1:g.20389C>T
NG_029043.1:g.4407C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4762C>T
ENST00000678492.1:n.4526C>T
Search 100 bp 5'
Search 100 bp 3'