Canonical Allele Identifier: CA434492131
Gene: GBE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.81627080G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81577929G>A , CM000665.2:g.81577929G>A GRCh38
NC_000003.11:g.81627080G>A , CM000665.1:g.81627080G>A GRCh37
NC_000003.10:g.81709770G>A NCBI36
NG_011810.1:g.188872C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000429644.7:c.1614C>T MANE Select ENSP00000410833.2:p.Phe538=
ENST00000429644.6:c.1614C>T ENSP00000410833.2:p.Phe538=
ENST00000484687.1:n.15C>T
ENST00000489715.1:c.1491C>T ENSP00000419638.1:p.Phe497=
NM_000158.3:c.1614C>T NP_000149.3:p.Phe538=
NM_000158.4:c.1614C>T MANE Select NP_000149.4:p.Phe538=
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