Canonical Allele Identifier: CA427441527
Gene: SUCLG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.84668464T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.84441340T>C , CM000664.2:g.84441340T>C GRCh38
NC_000002.11:g.84668464T>C , CM000664.1:g.84668464T>C GRCh37
NC_000002.10:g.84521975T>C NCBI36
NG_016755.1:g.23123A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000393868.7:c.438A>G MANE Select ENSP00000377446.2:p.Gly146=
ENST00000651342.1:c.438A>G ENSP00000498471.1:p.Gly146=
ENST00000393868.6:c.438A>G ENSP00000377446.2:p.Gly146=
ENST00000430989.1:n.478A>G
ENST00000442240.5:c.449A>G
ENST00000483605.5:n.517A>G
ENST00000491642.5:n.610A>G
NM_003849.3:c.438A>G NP_003840.2:p.Gly146=
NM_003849.4:c.438A>G MANE Select NP_003840.2:p.Gly146=
Search 100 bp 5'
Search 100 bp 3'