Canonical Allele Identifier: CA2697290098
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665966695

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214712A>G , CM000663.2:g.161214712A>G GRCh38
NC_000001.10:g.161184502A>G , CM000663.1:g.161184502A>G GRCh37
NC_000001.9:g.159451126A>G NCBI36
NG_013352.1:g.20398A>G
NG_029043.1:g.4416A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4771A>G
ENST00000678492.1:n.4535A>G