Canonical Allele Identifier: CA313056
Gene: SUCLG1 HGNC NCBI

Linked Data

ClinVar Variation Id: 203974
ClinVar RCV Id: RCV000186199
dbSNP Id: rs796052051
MyVariant Identifiers: chr2:g.84658681C>T (hg19) chr2:g.84431557C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.84431557C>T , CM000664.2:g.84431557C>T GRCh38
NC_000002.11:g.84658681C>T , CM000664.1:g.84658681C>T GRCh37
NC_000002.10:g.84512192C>T NCBI36
NG_016755.1:g.32906G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000393868.7:c.776G>A MANE Select ENSP00000377446.2:p.Gly259Asp
ENST00000651342.1:c.*216G>A ENSP00000498471.1:n.*216G>A
ENST00000393868.6:c.776G>A ENSP00000377446.2:p.Gly259Asp
ENST00000487809.1:n.523G>A
ENST00000491123.5:n.622G>A
NM_003849.3:c.776G>A NP_003840.2:p.Gly259Asp
NM_003849.4:c.776G>A MANE Select NP_003840.2:p.Gly259Asp
Search 100 bp 5'
Search 100 bp 3'