Canonical Allele Identifier: CA353688502
Gene: GBE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.81698142A>T (hg19) chr3:g.81648991A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81648991A>T , CM000665.2:g.81648991A>T GRCh38
NC_000003.11:g.81698142A>T , CM000665.1:g.81698142A>T GRCh37
NC_000003.10:g.81780832A>T NCBI36
NG_011810.1:g.117810T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.556T>A MANE Select ENSP00000410833.2:p.Phe186Ile
ENST00000429644.6:c.556T>A ENSP00000410833.2:p.Phe186Ile
ENST00000486920.1:n.552T>A
ENST00000489715.1:c.433T>A ENSP00000419638.1:p.Phe145Ile
ENST00000498468.1:n.84T>A
NM_000158.3:c.556T>A NP_000149.3:p.Phe186Ile
NM_000158.4:c.556T>A MANE Select NP_000149.4:p.Phe186Ile
Search 100 bp 5'
Search 100 bp 3'