Canonical Allele Identifier: CA353687865
Gene: GBE1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.81754717C>T (hg19) chr3:g.81705566C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.81705566C>T , CM000665.2:g.81705566C>T GRCh38
NC_000003.11:g.81754717C>T , CM000665.1:g.81754717C>T GRCh37
NC_000003.10:g.81837407C>T NCBI36
NG_011810.1:g.61235G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000429644.7:c.191G>A MANE Select ENSP00000410833.2:p.Gly64Asp
ENST00000429644.6:c.191G>A ENSP00000410833.2:p.Gly64Asp
ENST00000489715.1:c.68G>A ENSP00000419638.1:p.Gly23Asp
NM_000158.3:c.191G>A NP_000149.3:p.Gly64Asp
NM_000158.4:c.191G>A MANE Select NP_000149.4:p.Gly64Asp
Search 100 bp 5'
Search 100 bp 3'