Canonical Allele Identifier: CA2666624186
Gene: GBE1 HGNC NCBI

Linked Data

dbSNP Id: rs2107072602
gnomAD v4: 3-81649032-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81649032T>C , CM000665.2:g.81649032T>C GRCh38
NC_000003.11:g.81698183T>C , CM000665.1:g.81698183T>C GRCh37
NC_000003.10:g.81780873T>C NCBI36
NG_011810.1:g.117769A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.556-41A>G MANE Select ENSP00000410833.2:n.556-41A>G
ENST00000429644.6:c.556-41A>G ENSP00000410833.2:n.556-41A>G
ENST00000486920.1:n.552-41A>G
ENST00000489715.1:c.433-41A>G ENSP00000419638.1:n.433-41A>G
ENST00000498468.1:n.84-41A>G
NM_000158.3:c.556-41A>G NP_000149.3:n.556-41A>G
NM_000158.4:c.556-41A>G MANE Select NP_000149.4:n.556-41A>G