Canonical Allele Identifier: CA399656178
Gene: G6PC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2977907
ClinVar RCV Id: RCV003834505
dbSNP Id: rs2056092654
gnomAD v4: 17-42911116-C-A
COSMIC: COSM6147025
MyVariant Identifiers: chr17:g.41063133C>A (hg19) chr17:g.42911116C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42911116C>A , CM000679.2:g.42911116C>A GRCh38
NC_000017.10:g.41063133C>A , CM000679.1:g.41063133C>A GRCh37
NC_000017.9:g.38316659C>A NCBI36
NG_011808.1:g.15319C>A , LRG_147:g.15319C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000253801.7:c.764C>A MANE Select ENSP00000253801.1:p.Thr255Asn
ENST00000253801.6:c.764C>A ENSP00000253801.1:p.Thr255Asn
ENST00000585489.1:c.*156C>A ENSP00000466202.1:n.*156C>A
ENST00000592383.5:c.*156C>A ENSP00000465958.1:n.*156C>A
NM_000151.3:c.764C>A NP_000142.2:p.Thr255Asn
NM_001270397.1:c.*156C>A NP_001257326.1:n.*156C>A
NM_000151.4:c.764C>A MANE Select NP_000142.2:p.Thr255Asn
NM_001270397.2:c.*156C>A NP_001257326.1:n.*156C>A
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