Canonical Allele Identifier: CA500229329
Gene: G6PC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.41052971C>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42900954C>G , CM000679.2:g.42900954C>G GRCh38
NC_000017.10:g.41052971C>G , CM000679.1:g.41052971C>G GRCh37
NC_000017.9:g.38306497C>G NCBI36
NG_011808.1:g.5157C>G , LRG_147:g.5157C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.78C>G MANE Select ENSP00000253801.1:p.Ser26=
ENST00000253801.6:c.78C>G ENSP00000253801.1:p.Ser26=
ENST00000585489.1:c.78C>G ENSP00000466202.1:p.Ser26=
ENST00000588481.1:n.143C>G
ENST00000592383.5:c.78C>G ENSP00000465958.1:p.Ser26=
NM_000151.3:c.78C>G NP_000142.2:p.Ser26=
NM_001270397.1:c.78C>G NP_001257326.1:p.Ser26=
NM_000151.4:c.78C>G MANE Select NP_000142.2:p.Ser26=
NM_001270397.2:c.78C>G NP_001257326.1:p.Ser26=
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