Canonical Allele Identifier: CA500102263
Gene: G6PC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.41055969A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42903952A>C , CM000679.2:g.42903952A>C GRCh38
NC_000017.10:g.41055969A>C , CM000679.1:g.41055969A>C GRCh37
NC_000017.9:g.38309495A>C NCBI36
NG_011808.1:g.8155A>C , LRG_147:g.8155A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000253801.7:c.252A>C MANE Select ENSP00000253801.1:p.Pro84=
ENST00000253801.6:c.252A>C ENSP00000253801.1:p.Pro84=
ENST00000585489.1:c.252A>C ENSP00000466202.1:p.Pro84=
ENST00000588481.1:n.317A>C
ENST00000592383.5:c.252A>C ENSP00000465958.1:p.Pro84=
NM_000151.3:c.252A>C NP_000142.2:p.Pro84=
NM_001270397.1:c.252A>C NP_001257326.1:p.Pro84=
NM_000151.4:c.252A>C MANE Select NP_000142.2:p.Pro84=
NM_001270397.2:c.252A>C NP_001257326.1:p.Pro84=
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