Canonical Allele Identifier: CA2666604672
Gene: GBE1 HGNC NCBI

Linked Data

gnomAD v4: 3-81577886-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81577886T>C , CM000665.2:g.81577886T>C GRCh38
NC_000003.11:g.81627037T>C , CM000665.1:g.81627037T>C GRCh37
NC_000003.10:g.81709727T>C NCBI36
NG_011810.1:g.188915A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.1618+39A>G MANE Select ENSP00000410833.2:n.1618+39A>G
ENST00000429644.6:c.1618+39A>G ENSP00000410833.2:n.1618+39A>G
ENST00000484687.1:n.19+39A>G
ENST00000489715.1:c.1495+39A>G ENSP00000419638.1:n.1495+39A>G
NM_000158.3:c.1618+39A>G NP_000149.3:n.1618+39A>G
NM_000158.4:c.1618+39A>G MANE Select NP_000149.4:n.1618+39A>G