Canonical Allele Identifier: CA627768495

Gene: GCGR

Linked Data

• dbSNP Id: rs1242527268
• gnomAD v2: 17-79767766-C-T
• gnomAD v4: 17-81809890-C-T
• MyVariant Identifiers: chr17:g.79767766C>T (hg19) ; chr17:g.81809890C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809890C>T , CM000679.2:g.81809890C>T	GRCh38
NC_000017.10:g.79767766C>T , CM000679.1:g.79767766C>T	GRCh37
NG_016409.1:g.8717C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.163+6C>T MANE Select	ENSP00000383558.3:n.163+6C>T
ENST00000400723.7:c.163+6C>T	ENSP00000383558.3:n.163+6C>T
ENST00000570996.5:c.163+6C>T	ENSP00000460976.1:n.163+6C>T
ENST00000572185.1:n.464C>T
ENST00000573428.1:c.163+6C>T	ENSP00000458930.1:n.163+6C>T
ENST00000574283.2:n.103C>T
NM_000160.4:c.163+6C>T	NP_000151.1:n.163+6C>T
XM_006722277.1:c.163+6C>T	XP_006722340.1:n.163+6C>T
XM_011523539.1:c.-58C>T	XP_011521841.1:n.-58C>T
XM_011523540.1:c.-348C>T	XP_011521842.1:n.-348C>T
XM_017024446.1:c.157+6C>T	XP_016879935.1:n.157+6C>T
XM_017024447.1:c.-348C>T	XP_016879936.1:n.-348C>T
NM_000160.5:c.163+6C>T MANE Select	NP_000151.1:n.163+6C>T