Canonical Allele Identifier: CA627768189

Gene: GCGR

Linked Data

• dbSNP Id: rs1442480043
• gnomAD v2: 17-79767505-G-A
• gnomAD v3: 17-81809629-G-A
• gnomAD v4: 17-81809629-G-A
• MyVariant Identifiers: chr17:g.79767505G>A (hg19) ; chr17:g.81809629G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809629G>A , CM000679.2:g.81809629G>A	GRCh38
NC_000017.10:g.79767505G>A , CM000679.1:g.79767505G>A	GRCh37
NG_016409.1:g.8456G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-153G>A MANE Select	ENSP00000383558.3:n.61-153G>A
ENST00000400723.7:c.61-153G>A	ENSP00000383558.3:n.61-153G>A
ENST00000570996.5:c.61-153G>A	ENSP00000460976.1:n.61-153G>A
ENST00000572185.1:n.356-153G>A
ENST00000573428.1:c.61-153G>A	ENSP00000458930.1:n.61-153G>A
NM_000160.4:c.61-153G>A	NP_000151.1:n.61-153G>A
XM_006722277.1:c.61-153G>A	XP_006722340.1:n.61-153G>A
XM_011523539.1:c.-166-153G>A	XP_011521841.1:n.-166-153G>A
XM_011523540.1:c.-456-153G>A	XP_011521842.1:n.-456-153G>A
XM_017024446.1:c.61-159G>A	XP_016879935.1:n.61-159G>A
XM_017024447.1:c.-450-159G>A	XP_016879936.1:n.-450-159G>A
NM_000160.5:c.61-153G>A MANE Select	NP_000151.1:n.61-153G>A