Canonical Allele Identifier: CA2573137462
Gene: GBE1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1531206
ClinVar RCV Id: RCV002092352
dbSNP Id: rs2107066201
gnomAD v4: 3-81646492-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81646492G>C , CM000665.2:g.81646492G>C GRCh38
NC_000003.11:g.81695643G>C , CM000665.1:g.81695643G>C GRCh37
NC_000003.10:g.81778333G>C NCBI36
NG_011810.1:g.120309C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.692-10C>G MANE Select ENSP00000410833.2:n.692-10C>G
ENST00000429644.6:c.692-10C>G ENSP00000410833.2:n.692-10C>G
ENST00000489715.1:c.569-10C>G ENSP00000419638.1:n.569-10C>G
ENST00000498468.1:n.232C>G
NM_000158.3:c.692-10C>G NP_000149.3:n.692-10C>G
NM_000158.4:c.692-10C>G MANE Select NP_000149.4:n.692-10C>G