Canonical Allele Identifier: CA775687579

Gene: GCGR

Linked Data

• dbSNP Id: rs1354441882
• MyVariant Identifiers: chr17:g.79767498T>C (hg19) ; chr17:g.81809622T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809622T>C , CM000679.2:g.81809622T>C	GRCh38
NC_000017.10:g.79767498T>C , CM000679.1:g.79767498T>C	GRCh37
NG_016409.1:g.8449T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.61-160T>C MANE Select	ENSP00000383558.3:n.61-160T>C
ENST00000400723.7:c.61-160T>C	ENSP00000383558.3:n.61-160T>C
ENST00000570996.5:c.61-160T>C	ENSP00000460976.1:n.61-160T>C
ENST00000572185.1:n.356-160T>C
ENST00000573428.1:c.61-160T>C	ENSP00000458930.1:n.61-160T>C
NM_000160.4:c.61-160T>C	NP_000151.1:n.61-160T>C
XM_006722277.1:c.61-160T>C	XP_006722340.1:n.61-160T>C
XM_011523539.1:c.-166-160T>C	XP_011521841.1:n.-166-160T>C
XM_011523540.1:c.-456-160T>C	XP_011521842.1:n.-456-160T>C
XM_017024446.1:c.61-166T>C	XP_016879935.1:n.61-166T>C
XM_017024447.1:c.-450-166T>C	XP_016879936.1:n.-450-166T>C
NM_000160.5:c.61-160T>C MANE Select	NP_000151.1:n.61-160T>C