Canonical Allele Identifier: CA399657671
Gene: G6PC1 HGNC NCBI

Linked Data

dbSNP Id: rs2056095309

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42911375C>G , CM000679.2:g.42911375C>G GRCh38
NC_000017.10:g.41063392C>G , CM000679.1:g.41063392C>G GRCh37
NC_000017.9:g.38316918C>G NCBI36
NG_011808.1:g.15578C>G , LRG_147:g.15578C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.1023C>G MANE Select ENSP00000253801.1:p.Ile341Met
ENST00000253801.6:c.1023C>G ENSP00000253801.1:p.Ile341Met
ENST00000585489.1:c.*415C>G ENSP00000466202.1:n.*415C>G
NM_000151.3:c.1023C>G NP_000142.2:p.Ile341Met
NM_001270397.1:c.*415C>G NP_001257326.1:n.*415C>G
NM_000151.4:c.1023C>G MANE Select NP_000142.2:p.Ile341Met
NM_001270397.2:c.*415C>G NP_001257326.1:n.*415C>G