Canonical Allele Identifier: CA434492500
Gene: GBE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.81627170A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81578019A>C , CM000665.2:g.81578019A>C GRCh38
NC_000003.11:g.81627170A>C , CM000665.1:g.81627170A>C GRCh37
NC_000003.10:g.81709860A>C NCBI36
NG_011810.1:g.188782T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.1524T>G MANE Select ENSP00000410833.2:p.Pro508=
ENST00000429644.6:c.1524T>G ENSP00000410833.2:p.Pro508=
ENST00000489715.1:c.1401T>G ENSP00000419638.1:p.Pro467=
NM_000158.3:c.1524T>G NP_000149.3:p.Pro508=
NM_000158.4:c.1524T>G MANE Select NP_000149.4:p.Pro508=
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