Canonical Allele Identifier: CA353688204
Gene: GBE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.81695634C>G (hg19) chr3:g.81646483C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81646483C>G , CM000665.2:g.81646483C>G GRCh38
NC_000003.11:g.81695634C>G , CM000665.1:g.81695634C>G GRCh37
NC_000003.10:g.81778324C>G NCBI36
NG_011810.1:g.120318G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000429644.7:c.692-1G>C MANE Select ENSP00000410833.2:n.692-1G>C
ENST00000429644.6:c.692-1G>C ENSP00000410833.2:n.692-1G>C
ENST00000489715.1:c.569-1G>C ENSP00000419638.1:n.569-1G>C
ENST00000498468.1:n.241G>C
NM_000158.3:c.692-1G>C NP_000149.3:n.692-1G>C
NM_000158.4:c.692-1G>C MANE Select NP_000149.4:n.692-1G>C
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