Canonical Allele Identifier: CA890190011
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs1238116705
MyVariant Identifiers: chr1:g.161184479G>A (hg19) chr1:g.161214689G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214689G>A , CM000663.2:g.161214689G>A GRCh38
NC_000001.10:g.161184479G>A , CM000663.1:g.161184479G>A GRCh37
NC_000001.9:g.159451103G>A NCBI36
NG_013352.1:g.20375G>A
NG_029043.1:g.4393G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4748G>A
ENST00000678492.1:n.4512G>A
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