Canonical Allele Identifier: CA353686129
Gene: GBE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.81584412A>G (hg19) chr3:g.81535261A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81535261A>G , CM000665.2:g.81535261A>G GRCh38
NC_000003.11:g.81584412A>G , CM000665.1:g.81584412A>G GRCh37
NC_000003.10:g.81667102A>G NCBI36
NG_011810.1:g.231540T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.1868T>C MANE Select ENSP00000410833.2:p.Phe623Ser
ENST00000429644.6:c.1868T>C ENSP00000410833.2:p.Phe623Ser
ENST00000484687.1:n.269T>C
ENST00000489715.1:c.1745T>C ENSP00000419638.1:p.Phe582Ser
NM_000158.3:c.1868T>C NP_000149.3:p.Phe623Ser
NM_000158.4:c.1868T>C MANE Select NP_000149.4:p.Phe623Ser
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