Canonical Allele Identifier: CA434493977
Gene: GBE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.81695608T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81646457T>G , CM000665.2:g.81646457T>G GRCh38
NC_000003.11:g.81695608T>G , CM000665.1:g.81695608T>G GRCh37
NC_000003.10:g.81778298T>G NCBI36
NG_011810.1:g.120344A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.717A>C MANE Select ENSP00000410833.2:p.Ala239=
ENST00000429644.6:c.717A>C ENSP00000410833.2:p.Ala239=
ENST00000489715.1:c.594A>C ENSP00000419638.1:p.Ala198=
ENST00000498468.1:n.267A>C
NM_000158.3:c.717A>C NP_000149.3:p.Ala239=
NM_000158.4:c.717A>C MANE Select NP_000149.4:p.Ala239=
Search 100 bp 5'
Search 100 bp 3'