Canonical Allele Identifier: CA8587530
Gene: G6PC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2069743
dbSNP Id: rs771864998

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42903969A>G , CM000679.2:g.42903969A>G GRCh38
NC_000017.10:g.41055986A>G , CM000679.1:g.41055986A>G GRCh37
NC_000017.9:g.38309512A>G NCBI36
NG_011808.1:g.8172A>G , LRG_147:g.8172A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.269A>G MANE Select ENSP00000253801.1:p.Asp90Gly
ENST00000253801.6:c.269A>G ENSP00000253801.1:p.Asp90Gly
ENST00000585489.1:c.269A>G ENSP00000466202.1:p.Asp90Gly
ENST00000588481.1:n.334A>G
ENST00000592383.5:c.269A>G ENSP00000465958.1:p.Asp90Gly
NM_000151.3:c.269A>G NP_000142.2:p.Asp90Gly
NM_001270397.1:c.269A>G NP_001257326.1:p.Asp90Gly
NM_000151.4:c.269A>G MANE Select NP_000142.2:p.Asp90Gly
NM_001270397.2:c.269A>G NP_001257326.1:p.Asp90Gly