Canonical Allele Identifier: CA126242
Gene: GCGR HGNC NCBI

Linked Data

ClinVar Variation Id: 16159
ClinVar RCV Id: RCV000017542 RCV000950476
dbSNP Id: rs1801483
ExAC: 17:79767715 G / A
gnomAD v2: 17-79767715-G-A
gnomAD v3: 17-81809839-G-A
gnomAD v4: 17-81809839-G-A
MyVariant Identifiers: chr17:g.79767715G>A (hg19) chr17:g.81809839G>A (hg38)
PubMed: PMID:7773293 PMID:8563746
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81809839G>A , CM000679.2:g.81809839G>A GRCh38
NC_000017.10:g.79767715G>A , CM000679.1:g.79767715G>A GRCh37
NG_016409.1:g.8666G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000400723.8:c.118G>A MANE Select ENSP00000383558.3:p.Gly40Ser
ENST00000400723.7:c.118G>A ENSP00000383558.3:p.Gly40Ser
ENST00000570996.5:c.118G>A ENSP00000460976.1:p.Gly40Ser
ENST00000572185.1:n.413G>A
ENST00000573428.1:c.118G>A ENSP00000458930.1:p.Gly40Ser
ENST00000574283.2:n.52G>A
NM_000160.4:c.118G>A NP_000151.1:p.Gly40Ser
XM_006722277.1:c.118G>A XP_006722340.1:p.Gly40Ser
XM_011523539.1:c.-109G>A XP_011521841.1:n.-109G>A
XM_011523540.1:c.-399G>A XP_011521842.1:n.-399G>A
XM_017024446.1:c.112G>A XP_016879935.1:p.Gly38Ser
XM_017024447.1:c.-399G>A XP_016879936.1:n.-399G>A
NM_000160.5:c.118G>A MANE Select NP_000151.1:p.Gly40Ser
Search 100 bp 5'
Search 100 bp 3'