Canonical Allele Identifier: CA1202648729
Gene: NDUFS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161214693T= , CM000663.2:g.161214693T= GRCh38
NC_000001.10:g.161184483T= , CM000663.1:g.161184483T= GRCh37
NC_000001.9:g.159451107T= NCBI36
NG_013352.1:g.20379T=
NG_029043.1:g.4397T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000677577.1:n.4752T=
ENST00000678492.1:n.4516T=