Canonical Allele Identifier: CA890190003
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs1161740855
MyVariant Identifiers: chr1:g.161184464A>G (hg19) chr1:g.161214674A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214674A>G , CM000663.2:g.161214674A>G GRCh38
NC_000001.10:g.161184464A>G , CM000663.1:g.161184464A>G GRCh37
NC_000001.9:g.159451088A>G NCBI36
NG_013352.1:g.20360A>G
NG_029043.1:g.4378A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4733A>G
ENST00000678492.1:n.4497A>G
Search 100 bp 5'
Search 100 bp 3'