Canonical Allele Identifier: CA353687767
Gene: GBE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.81754671G>C (hg19) chr3:g.81705520G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81705520G>C , CM000665.2:g.81705520G>C GRCh38
NC_000003.11:g.81754671G>C , CM000665.1:g.81754671G>C GRCh37
NC_000003.10:g.81837361G>C NCBI36
NG_011810.1:g.61281C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.237C>G MANE Select ENSP00000410833.2:p.His79Gln
ENST00000429644.6:c.237C>G ENSP00000410833.2:p.His79Gln
ENST00000489715.1:c.114C>G ENSP00000419638.1:p.His38Gln
NM_000158.3:c.237C>G NP_000149.3:p.His79Gln
NM_000158.4:c.237C>G MANE Select NP_000149.4:p.His79Gln
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