Canonical Allele Identifier: CA295097859

Gene: GCGR

Linked Data

• dbSNP Id: rs765309084
• gnomAD v2: 17-79767534-T-C
• gnomAD v3: 17-81809658-T-C
• gnomAD v4: 17-81809658-T-C
• MyVariant Identifiers: chr17:g.79767534T>C (hg19) ; chr17:g.81809658T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809658T>C , CM000679.2:g.81809658T>C	GRCh38
NC_000017.10:g.79767534T>C , CM000679.1:g.79767534T>C	GRCh37
NG_016409.1:g.8485T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-124T>C MANE Select	ENSP00000383558.3:n.61-124T>C
ENST00000400723.7:c.61-124T>C	ENSP00000383558.3:n.61-124T>C
ENST00000570996.5:c.61-124T>C	ENSP00000460976.1:n.61-124T>C
ENST00000572185.1:n.356-124T>C
ENST00000573428.1:c.61-124T>C	ENSP00000458930.1:n.61-124T>C
NM_000160.4:c.61-124T>C	NP_000151.1:n.61-124T>C
XM_006722277.1:c.61-124T>C	XP_006722340.1:n.61-124T>C
XM_011523539.1:c.-166-124T>C	XP_011521841.1:n.-166-124T>C
XM_011523540.1:c.-456-124T>C	XP_011521842.1:n.-456-124T>C
XM_017024446.1:c.61-130T>C	XP_016879935.1:n.61-130T>C
XM_017024447.1:c.-450-130T>C	XP_016879936.1:n.-450-130T>C
NM_000160.5:c.61-124T>C MANE Select	NP_000151.1:n.61-124T>C