Canonical Allele Identifier: CA427119102
Gene: SUCLG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.84658758T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.84431634T>C , CM000664.2:g.84431634T>C GRCh38
NC_000002.11:g.84658758T>C , CM000664.1:g.84658758T>C GRCh37
NC_000002.10:g.84512269T>C NCBI36
NG_016755.1:g.32829A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000393868.7:c.699A>G MANE Select ENSP00000377446.2:p.Gly233=
ENST00000651342.1:c.*139A>G ENSP00000498471.1:n.*139A>G
ENST00000393868.6:c.699A>G ENSP00000377446.2:p.Gly233=
ENST00000487809.1:n.446A>G
ENST00000491123.5:n.545A>G
NM_003849.3:c.699A>G NP_003840.2:p.Gly233=
NM_003849.4:c.699A>G MANE Select NP_003840.2:p.Gly233=
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Search 100 bp 3'