Canonical Allele Identifier: CA1378760175
Gene: GBE1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81705544T= , CM000665.2:g.81705544T= GRCh38
NC_000003.11:g.81754695T= , CM000665.1:g.81754695T= GRCh37
NC_000003.10:g.81837385T= NCBI36
NG_011810.1:g.61257A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.213A= MANE Select ENSP00000410833.2:p.Arg71=
ENST00000429644.6:c.213A= ENSP00000410833.2:p.Arg71=
ENST00000489715.1:c.90A= ENSP00000419638.1:p.Arg30=
NM_000158.3:c.213A= NP_000149.3:p.Arg71=
NM_000158.4:c.213A= MANE Select NP_000149.4:p.Arg71=
Search 100 bp 5'
Search 100 bp 3'