Canonical Allele Identifier: CA353686112
Gene: GBE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.81584405G>C (hg19) chr3:g.81535254G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81535254G>C , CM000665.2:g.81535254G>C GRCh38
NC_000003.11:g.81584405G>C , CM000665.1:g.81584405G>C GRCh37
NC_000003.10:g.81667095G>C NCBI36
NG_011810.1:g.231547C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000429644.7:c.1875C>G MANE Select ENSP00000410833.2:p.Phe625Leu
ENST00000429644.6:c.1875C>G ENSP00000410833.2:p.Phe625Leu
ENST00000484687.1:n.276C>G
ENST00000489715.1:c.1752C>G ENSP00000419638.1:p.Phe584Leu
NM_000158.3:c.1875C>G NP_000149.3:p.Phe625Leu
NM_000158.4:c.1875C>G MANE Select NP_000149.4:p.Phe625Leu
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