Canonical Allele Identifier: CA430939863
Gene: NDUFS1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.206986922C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.206122198C>A , CM000664.2:g.206122198C>A GRCh38
NC_000002.11:g.206986922C>A , CM000664.1:g.206986922C>A GRCh37
NC_000002.10:g.206695167C>A NCBI36
NG_009248.1:g.42266G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000233190.11:c.*1987G>T MANE Select ENSP00000233190.5:n.*1987G>T
ENST00000233190.10:c.*1987G>T ENSP00000233190.5:n.*1987G>T
NM_001199981.2:c.*1987G>T NP_001186910.1:n.*1987G>T
NM_001199982.2:c.*1987G>T NP_001186911.1:n.*1987G>T
NM_001199983.2:c.*1987G>T NP_001186912.1:n.*1987G>T
NM_005006.7:c.*1987G>T MANE Select NP_004997.4:n.*1987G>T
NM_001199984.2:c.*1987G>T NP_001186913.1:n.*1987G>T