Canonical Allele Identifier: CA1202648716
Gene: NDUFS2 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4733A=
ENST00000678492.1:n.4497A=