Canonical Allele Identifier: CA78298519
Gene: GBE1 HGNC NCBI

Linked Data

dbSNP Id: rs987689345
gnomAD v3: 3-81705671-T-C
gnomAD v4: 3-81705671-T-C
MyVariant Identifiers: chr3:g.81754822T>C (hg19) chr3:g.81705671T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81705671T>C , CM000665.2:g.81705671T>C GRCh38
NC_000003.11:g.81754822T>C , CM000665.1:g.81754822T>C GRCh37
NC_000003.10:g.81837512T>C NCBI36
NG_011810.1:g.61130A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.144-58A>G MANE Select ENSP00000410833.2:n.144-58A>G
ENST00000429644.6:c.144-58A>G ENSP00000410833.2:n.144-58A>G
ENST00000489715.1:c.21-58A>G ENSP00000419638.1:n.21-58A>G
NM_000158.3:c.144-58A>G NP_000149.3:n.144-58A>G
NM_000158.4:c.144-58A>G MANE Select NP_000149.4:n.144-58A>G
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