Canonical Allele Identifier: CA434494095
Gene: GBE1 HGNC NCBI

Linked Data

gnomAD v4: 3-81648977-T-C
MyVariant Identifiers: chr3:g.81698128T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81648977T>C , CM000665.2:g.81648977T>C GRCh38
NC_000003.11:g.81698128T>C , CM000665.1:g.81698128T>C GRCh37
NC_000003.10:g.81780818T>C NCBI36
NG_011810.1:g.117824A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.570A>G MANE Select ENSP00000410833.2:p.Arg190=
ENST00000429644.6:c.570A>G ENSP00000410833.2:p.Arg190=
ENST00000486920.1:n.566A>G
ENST00000489715.1:c.447A>G ENSP00000419638.1:p.Arg149=
ENST00000498468.1:n.98A>G
NM_000158.3:c.570A>G NP_000149.3:p.Arg190=
NM_000158.4:c.570A>G MANE Select NP_000149.4:p.Arg190=