Canonical Allele Identifier: CA775687775

Gene: GCGR

Linked Data

• dbSNP Id: rs1368707704
• gnomAD v4: 17-81809727-C-G
• MyVariant Identifiers: chr17:g.79767603C>G (hg19) ; chr17:g.81809727C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809727C>G , CM000679.2:g.81809727C>G	GRCh38
NC_000017.10:g.79767603C>G , CM000679.1:g.79767603C>G	GRCh37
NG_016409.1:g.8554C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-55C>G MANE Select	ENSP00000383558.3:n.61-55C>G
ENST00000400723.7:c.61-55C>G	ENSP00000383558.3:n.61-55C>G
ENST00000570996.5:c.61-55C>G	ENSP00000460976.1:n.61-55C>G
ENST00000572185.1:n.356-55C>G
ENST00000573428.1:c.61-55C>G	ENSP00000458930.1:n.61-55C>G
NM_000160.4:c.61-55C>G	NP_000151.1:n.61-55C>G
XM_006722277.1:c.61-55C>G	XP_006722340.1:n.61-55C>G
XM_011523539.1:c.-166-55C>G	XP_011521841.1:n.-166-55C>G
XM_011523540.1:c.-456-55C>G	XP_011521842.1:n.-456-55C>G
XM_017024446.1:c.61-61C>G	XP_016879935.1:n.61-61C>G
XM_017024447.1:c.-450-61C>G	XP_016879936.1:n.-450-61C>G
NM_000160.5:c.61-55C>G MANE Select	NP_000151.1:n.61-55C>G