Canonical Allele Identifier: CA8587676
Gene: G6PC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 723357
ClinVar RCV Id: RCV000897106 RCV004028469
dbSNP Id: rs141352548
ExAC: 17:41063311 C / G
gnomAD v2: 17-41063311-C-G
gnomAD v3: 17-42911294-C-G
gnomAD v4: 17-42911294-C-G
MyVariant Identifiers: chr17:g.41063311C>G (hg19) chr17:g.42911294C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42911294C>G , CM000679.2:g.42911294C>G GRCh38
NC_000017.10:g.41063311C>G , CM000679.1:g.41063311C>G GRCh37
NC_000017.9:g.38316837C>G NCBI36
NG_011808.1:g.15497C>G , LRG_147:g.15497C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.942C>G MANE Select ENSP00000253801.1:p.Pro314=
ENST00000253801.6:c.942C>G ENSP00000253801.1:p.Pro314=
ENST00000585489.1:c.*334C>G ENSP00000466202.1:n.*334C>G
ENST00000592383.5:c.*334C>G ENSP00000465958.1:n.*334C>G
NM_000151.3:c.942C>G NP_000142.2:p.Pro314=
NM_001270397.1:c.*334C>G NP_001257326.1:n.*334C>G
NM_000151.4:c.942C>G MANE Select NP_000142.2:p.Pro314=
NM_001270397.2:c.*334C>G NP_001257326.1:n.*334C>G
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