Canonical Allele Identifier: CA401491275

Gene: GCGR

Linked Data

• MyVariant Identifiers: chr17:g.79767716G>T (hg19) ; chr17:g.81809840G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809840G>T , CM000679.2:g.81809840G>T	GRCh38
NC_000017.10:g.79767716G>T , CM000679.1:g.79767716G>T	GRCh37
NG_016409.1:g.8667G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000400723.8:c.119G>T MANE Select	ENSP00000383558.3:p.Gly40Val
ENST00000400723.7:c.119G>T	ENSP00000383558.3:p.Gly40Val
ENST00000570996.5:c.119G>T	ENSP00000460976.1:p.Gly40Val
ENST00000572185.1:n.414G>T
ENST00000573428.1:c.119G>T	ENSP00000458930.1:p.Gly40Val
ENST00000574283.2:n.53G>T
NM_000160.4:c.119G>T	NP_000151.1:p.Gly40Val
XM_006722277.1:c.119G>T	XP_006722340.1:p.Gly40Val
XM_011523539.1:c.-108G>T	XP_011521841.1:n.-108G>T
XM_011523540.1:c.-398G>T	XP_011521842.1:n.-398G>T
XM_017024446.1:c.113G>T	XP_016879935.1:p.Gly38Val
XM_017024447.1:c.-398G>T	XP_016879936.1:n.-398G>T
NM_000160.5:c.119G>T MANE Select	NP_000151.1:p.Gly40Val