Canonical Allele Identifier: CA986871662

Gene: GCGR

Linked Data

• dbSNP Id: rs2038049931
• gnomAD v3: 17-81809640-T-C
• gnomAD v4: 17-81809640-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809640T>C , CM000679.2:g.81809640T>C	GRCh38
NC_000017.10:g.79767516T>C , CM000679.1:g.79767516T>C	GRCh37
NG_016409.1:g.8467T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-142T>C MANE Select	ENSP00000383558.3:n.61-142T>C
ENST00000400723.7:c.61-142T>C	ENSP00000383558.3:n.61-142T>C
ENST00000570996.5:c.61-142T>C	ENSP00000460976.1:n.61-142T>C
ENST00000572185.1:n.356-142T>C
ENST00000573428.1:c.61-142T>C	ENSP00000458930.1:n.61-142T>C
NM_000160.4:c.61-142T>C	NP_000151.1:n.61-142T>C
XM_006722277.1:c.61-142T>C	XP_006722340.1:n.61-142T>C
XM_011523539.1:c.-166-142T>C	XP_011521841.1:n.-166-142T>C
XM_011523540.1:c.-456-142T>C	XP_011521842.1:n.-456-142T>C
XM_017024446.1:c.61-148T>C	XP_016879935.1:n.61-148T>C
XM_017024447.1:c.-450-148T>C	XP_016879936.1:n.-450-148T>C
NM_000160.5:c.61-142T>C MANE Select	NP_000151.1:n.61-142T>C