Canonical Allele Identifier: CA401491348

Gene: GCGR

Linked Data

• MyVariant Identifiers: chr17:g.79767723G>T (hg19) ; chr17:g.81809847G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809847G>T , CM000679.2:g.81809847G>T	GRCh38
NC_000017.10:g.79767723G>T , CM000679.1:g.79767723G>T	GRCh37
NG_016409.1:g.8674G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000400723.8:c.126G>T MANE Select	ENSP00000383558.3:p.Gln42His
ENST00000400723.7:c.126G>T	ENSP00000383558.3:p.Gln42His
ENST00000570996.5:c.126G>T	ENSP00000460976.1:p.Gln42His
ENST00000572185.1:n.421G>T
ENST00000573428.1:c.126G>T	ENSP00000458930.1:p.Gln42His
ENST00000574283.2:n.60G>T
NM_000160.4:c.126G>T	NP_000151.1:p.Gln42His
XM_006722277.1:c.126G>T	XP_006722340.1:p.Gln42His
XM_011523539.1:c.-101G>T	XP_011521841.1:n.-101G>T
XM_011523540.1:c.-391G>T	XP_011521842.1:n.-391G>T
XM_017024446.1:c.120G>T	XP_016879935.1:p.Gln40His
XM_017024447.1:c.-391G>T	XP_016879936.1:n.-391G>T
NM_000160.5:c.126G>T MANE Select	NP_000151.1:p.Gln42His