Canonical Allele Identifier: CA772150999
Gene: G6PC1 HGNC NCBI

Linked Data

dbSNP Id: rs1398370649
gnomAD v3: 17-42911427-G-T
gnomAD v4: 17-42911427-G-T
MyVariant Identifiers: chr17:g.41063444G>T (hg19) chr17:g.42911427G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42911427G>T , CM000679.2:g.42911427G>T GRCh38
NC_000017.10:g.41063444G>T , CM000679.1:g.41063444G>T GRCh37
NC_000017.9:g.38316970G>T NCBI36
NG_011808.1:g.15630G>T , LRG_147:g.15630G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000253801.7:c.*1G>T MANE Select ENSP00000253801.1:n.*1G>T
ENST00000253801.6:c.*1G>T ENSP00000253801.1:n.*1G>T
ENST00000585489.1:c.*467G>T ENSP00000466202.1:n.*467G>T
NM_000151.3:c.*1G>T NP_000142.2:n.*1G>T
NM_001270397.1:c.*467G>T NP_001257326.1:n.*467G>T
NM_000151.4:c.*1G>T MANE Select NP_000142.2:n.*1G>T
NM_001270397.2:c.*467G>T NP_001257326.1:n.*467G>T
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