Canonical Allele Identifier: CA427119069
Gene: SUCLG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.84658698T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.84431574T>G , CM000664.2:g.84431574T>G GRCh38
NC_000002.11:g.84658698T>G , CM000664.1:g.84658698T>G GRCh37
NC_000002.10:g.84512209T>G NCBI36
NG_016755.1:g.32889A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000393868.7:c.759A>C MANE Select ENSP00000377446.2:p.Ile253=
ENST00000651342.1:c.*199A>C ENSP00000498471.1:n.*199A>C
ENST00000393868.6:c.759A>C ENSP00000377446.2:p.Ile253=
ENST00000487809.1:n.506A>C
ENST00000491123.5:n.605A>C
NM_003849.3:c.759A>C NP_003840.2:p.Ile253=
NM_003849.4:c.759A>C MANE Select NP_003840.2:p.Ile253=