Canonical Allele Identifier: CA353688916
Gene: GBE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.81720038G>T (hg19) chr3:g.81670887G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81670887G>T , CM000665.2:g.81670887G>T GRCh38
NC_000003.11:g.81720038G>T , CM000665.1:g.81720038G>T GRCh37
NC_000003.10:g.81802728G>T NCBI36
NG_011810.1:g.95914C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.380C>A MANE Select ENSP00000410833.2:p.Pro127Gln
ENST00000429644.6:c.380C>A ENSP00000410833.2:p.Pro127Gln
ENST00000477426.1:n.96C>A
ENST00000489715.1:c.257C>A ENSP00000419638.1:p.Pro86Gln
NM_000158.3:c.380C>A NP_000149.3:p.Pro127Gln
NM_000158.4:c.380C>A MANE Select NP_000149.4:p.Pro127Gln
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