Canonical Allele Identifier: CA8587722
Gene: G6PC1 HGNC NCBI

Linked Data

dbSNP Id: rs765355094
ExAC: 17:41063477 A / G
gnomAD v2: 17-41063477-A-G
gnomAD v4: 17-42911460-A-G
MyVariant Identifiers: chr17:g.41063477A>G (hg19) chr17:g.42911460A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42911460A>G , CM000679.2:g.42911460A>G GRCh38
NC_000017.10:g.41063477A>G , CM000679.1:g.41063477A>G GRCh37
NC_000017.9:g.38317003A>G NCBI36
NG_011808.1:g.15663A>G , LRG_147:g.15663A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.*34A>G MANE Select ENSP00000253801.1:n.*34A>G
ENST00000253801.6:c.*34A>G ENSP00000253801.1:n.*34A>G
ENST00000585489.1:c.*500A>G ENSP00000466202.1:n.*500A>G
NM_000151.3:c.*34A>G NP_000142.2:n.*34A>G
NM_001270397.1:c.*500A>G NP_001257326.1:n.*500A>G
NM_000151.4:c.*34A>G MANE Select NP_000142.2:n.*34A>G
NM_001270397.2:c.*500A>G NP_001257326.1:n.*500A>G
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