Canonical Allele Identifier: CA2640508912

Gene: GCGR

Linked Data

• gnomAD v4: 17-81809926-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809926C>T , CM000679.2:g.81809926C>T	GRCh38
NC_000017.10:g.79767802C>T , CM000679.1:g.79767802C>T	GRCh37
NG_016409.1:g.8753C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.163+42C>T MANE Select	ENSP00000383558.3:n.163+42C>T
ENST00000400723.7:c.163+42C>T	ENSP00000383558.3:n.163+42C>T
ENST00000570996.5:c.163+42C>T	ENSP00000460976.1:n.163+42C>T
ENST00000572185.1:n.500C>T
ENST00000573428.1:c.163+42C>T	ENSP00000458930.1:n.163+42C>T
ENST00000574283.2:n.139C>T
NM_000160.4:c.163+42C>T	NP_000151.1:n.163+42C>T
XM_006722277.1:c.163+42C>T	XP_006722340.1:n.163+42C>T
XM_011523539.1:c.-22C>T	XP_011521841.1:n.-22C>T
XM_011523540.1:c.-312C>T	XP_011521842.1:n.-312C>T
XM_017024446.1:c.157+42C>T	XP_016879935.1:n.157+42C>T
XM_017024447.1:c.-312C>T	XP_016879936.1:n.-312C>T
NM_000160.5:c.163+42C>T MANE Select	NP_000151.1:n.163+42C>T