Canonical Allele Identifier: CA399654762
Gene: G6PC1 HGNC NCBI

Linked Data

dbSNP Id: rs1482292287

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42909328G>C , CM000679.2:g.42909328G>C GRCh38
NC_000017.10:g.41061345G>C , CM000679.1:g.41061345G>C GRCh37
NC_000017.9:g.38314871G>C NCBI36
NG_011808.1:g.13531G>C , LRG_147:g.13531G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.472G>C MANE Select ENSP00000253801.1:p.Gly158Arg
ENST00000253801.6:c.472G>C ENSP00000253801.1:p.Gly158Arg
ENST00000585489.1:c.447-1587G>C ENSP00000466202.1:n.447-1587G>C
ENST00000592383.5:c.395G>C ENSP00000465958.1:p.Gly132Ala
NM_000151.3:c.472G>C NP_000142.2:p.Gly158Arg
NM_001270397.1:c.395G>C NP_001257326.1:p.Gly132Ala
NM_000151.4:c.472G>C MANE Select NP_000142.2:p.Gly158Arg
NM_001270397.2:c.395G>C NP_001257326.1:p.Gly132Ala