Canonical Allele Identifier: CA2500048
Gene: GBE1 HGNC NCBI

Linked Data

dbSNP Id: rs760080170
gnomAD v2: 3-81754790-A-G
gnomAD v4: 3-81705639-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81705639A>G , CM000665.2:g.81705639A>G GRCh38
NC_000003.11:g.81754790A>G , CM000665.1:g.81754790A>G GRCh37
NC_000003.10:g.81837480A>G NCBI36
NG_011810.1:g.61162T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.144-26T>C MANE Select ENSP00000410833.2:n.144-26T>C
ENST00000429644.6:c.144-26T>C ENSP00000410833.2:n.144-26T>C
ENST00000489715.1:c.21-26T>C ENSP00000419638.1:n.21-26T>C
NM_000158.3:c.144-26T>C NP_000149.3:n.144-26T>C
NM_000158.4:c.144-26T>C MANE Select NP_000149.4:n.144-26T>C