Canonical Allele Identifier: CA434493996
Gene: GBE1 HGNC NCBI

Linked Data

gnomAD v4: 3-81648860-G-T
MyVariant Identifiers: chr3:g.81698011G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81648860G>T , CM000665.2:g.81648860G>T GRCh38
NC_000003.11:g.81698011G>T , CM000665.1:g.81698011G>T GRCh37
NC_000003.10:g.81780701G>T NCBI36
NG_011810.1:g.117941C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000429644.7:c.687C>A MANE Select ENSP00000410833.2:p.Gly229=
ENST00000429644.6:c.687C>A ENSP00000410833.2:p.Gly229=
ENST00000489715.1:c.564C>A ENSP00000419638.1:p.Gly188=
ENST00000498468.1:n.215C>A
NM_000158.3:c.687C>A NP_000149.3:p.Gly229=
NM_000158.4:c.687C>A MANE Select NP_000149.4:p.Gly229=
Search 100 bp 5'
Search 100 bp 3'