Canonical Allele Identifier: CA427119075
Gene: SUCLG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.84658704G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.84431580G>C , CM000664.2:g.84431580G>C GRCh38
NC_000002.11:g.84658704G>C , CM000664.1:g.84658704G>C GRCh37
NC_000002.10:g.84512215G>C NCBI36
NG_016755.1:g.32883C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000393868.7:c.753C>G MANE Select ENSP00000377446.2:p.Gly251=
ENST00000651342.1:c.*193C>G ENSP00000498471.1:n.*193C>G
ENST00000393868.6:c.753C>G ENSP00000377446.2:p.Gly251=
ENST00000487809.1:n.500C>G
ENST00000491123.5:n.599C>G
NM_003849.3:c.753C>G NP_003840.2:p.Gly251=
NM_003849.4:c.753C>G MANE Select NP_003840.2:p.Gly251=
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