Canonical Allele Identifier: CA2699918916
Gene: SUCLG1 HGNC NCBI

Linked Data

dbSNP Id: rs2104236376
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.84425268C>T , CM000664.2:g.84425268C>T GRCh38
NC_000002.11:g.84652392C>T , CM000664.1:g.84652392C>T GRCh37
NC_000002.10:g.84505903C>T NCBI36
NG_016755.1:g.39195G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000393868.7:c.1014+147G>A MANE Select ENSP00000377446.2:n.1014+147G>A
ENST00000651342.1:c.*454+147G>A ENSP00000498471.1:n.*454+147G>A
ENST00000393868.6:c.1014+147G>A ENSP00000377446.2:n.1014+147G>A
ENST00000484365.1:n.1522+147G>A
ENST00000491123.5:n.860+147G>A
NM_003849.3:c.1014+147G>A NP_003840.2:n.1014+147G>A
NM_003849.4:c.1014+147G>A MANE Select NP_003840.2:n.1014+147G>A
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