Canonical Allele Identifier: CA775687723

Gene: GCGR

Linked Data

• dbSNP Id: rs1186997704
• gnomAD v4: 17-81809721-G-A
• MyVariant Identifiers: chr17:g.79767597G>A (hg19) ; chr17:g.81809721G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809721G>A , CM000679.2:g.81809721G>A	GRCh38
NC_000017.10:g.79767597G>A , CM000679.1:g.79767597G>A	GRCh37
NG_016409.1:g.8548G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-61G>A MANE Select	ENSP00000383558.3:n.61-61G>A
ENST00000400723.7:c.61-61G>A	ENSP00000383558.3:n.61-61G>A
ENST00000570996.5:c.61-61G>A	ENSP00000460976.1:n.61-61G>A
ENST00000572185.1:n.356-61G>A
ENST00000573428.1:c.61-61G>A	ENSP00000458930.1:n.61-61G>A
NM_000160.4:c.61-61G>A	NP_000151.1:n.61-61G>A
XM_006722277.1:c.61-61G>A	XP_006722340.1:n.61-61G>A
XM_011523539.1:c.-166-61G>A	XP_011521841.1:n.-166-61G>A
XM_011523540.1:c.-456-61G>A	XP_011521842.1:n.-456-61G>A
XM_017024446.1:c.61-67G>A	XP_016879935.1:n.61-67G>A
XM_017024447.1:c.-450-67G>A	XP_016879936.1:n.-450-67G>A
NM_000160.5:c.61-61G>A MANE Select	NP_000151.1:n.61-61G>A