Canonical Allele Identifier: CA2500037
Gene: GBE1 HGNC NCBI

Linked Data

dbSNP Id: rs189658580
gnomAD v2: 3-81754712-T-C
gnomAD v3: 3-81705561-T-C
gnomAD v4: 3-81705561-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81705561T>C , CM000665.2:g.81705561T>C GRCh38
NC_000003.11:g.81754712T>C , CM000665.1:g.81754712T>C GRCh37
NC_000003.10:g.81837402T>C NCBI36
NG_011810.1:g.61240A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.196A>G MANE Select ENSP00000410833.2:p.Ile66Val
ENST00000429644.6:c.196A>G ENSP00000410833.2:p.Ile66Val
ENST00000489715.1:c.73A>G ENSP00000419638.1:p.Ile25Val
NM_000158.3:c.196A>G NP_000149.3:p.Ile66Val
NM_000158.4:c.196A>G MANE Select NP_000149.4:p.Ile66Val