Canonical Allele Identifier: CA1202648713
Gene: NDUFS2 HGNC NCBI

Linked Data

dbSNP Id: rs1665962511

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214670G>C , CM000663.2:g.161214670G>C GRCh38
NC_000001.10:g.161184460G>C , CM000663.1:g.161184460G>C GRCh37
NC_000001.9:g.159451084G>C NCBI36
NG_013352.1:g.20356G>C
NG_029043.1:g.4374G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4729G>C
ENST00000678492.1:n.4493G>C