Canonical Allele Identifier: CA2260696544
Gene: G6PC1 HGNC NCBI

Linked Data

dbSNP Id: rs2056079953

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42909086C>T , CM000679.2:g.42909086C>T GRCh38
NC_000017.10:g.41061103C>T , CM000679.1:g.41061103C>T GRCh37
NC_000017.9:g.38314629C>T NCBI36
NG_011808.1:g.13289C>T , LRG_147:g.13289C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.447-217C>T MANE Select ENSP00000253801.1:n.447-217C>T
ENST00000253801.6:c.447-217C>T ENSP00000253801.1:n.447-217C>T
ENST00000585489.1:c.446+1458C>T ENSP00000466202.1:n.446+1458C>T
ENST00000592383.5:c.370-217C>T ENSP00000465958.1:n.370-217C>T
NM_000151.3:c.447-217C>T NP_000142.2:n.447-217C>T
NM_001270397.1:c.370-217C>T NP_001257326.1:n.370-217C>T
NM_000151.4:c.447-217C>T MANE Select NP_000142.2:n.447-217C>T
NM_001270397.2:c.370-217C>T NP_001257326.1:n.370-217C>T