Canonical Allele Identifier: CA1378730140
Gene: GBE1 HGNC NCBI

Linked Data

dbSNP Id: rs1704803561

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81648767C>A , CM000665.2:g.81648767C>A GRCh38
NC_000003.11:g.81697918C>A , CM000665.1:g.81697918C>A GRCh37
NC_000003.10:g.81780608C>A NCBI36
NG_011810.1:g.118034G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000429644.7:c.691+89G>T MANE Select ENSP00000410833.2:n.691+89G>T
ENST00000429644.6:c.691+89G>T ENSP00000410833.2:n.691+89G>T
ENST00000489715.1:c.568+89G>T ENSP00000419638.1:n.568+89G>T
ENST00000498468.1:n.219+89G>T
NM_000158.3:c.691+89G>T NP_000149.3:n.691+89G>T
NM_000158.4:c.691+89G>T MANE Select NP_000149.4:n.691+89G>T