Canonical Allele Identifier: CA627768198
Gene: GCGR HGNC NCBI

Linked Data

dbSNP Id: rs1360566146
gnomAD v2: 17-79767514-T-C
gnomAD v3: 17-81809638-T-C
gnomAD v4: 17-81809638-T-C
MyVariant Identifiers: chr17:g.79767514T>C (hg19) chr17:g.79767514_79767522delinsCCTGTCTGC (hg19) chr17:g.81809638T>C (hg38) chr17:g.81809638_81809646delinsCCTGTCTGC (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.81809638T>C , CM000679.2:g.81809638T>C GRCh38
NC_000017.10:g.79767514T>C , CM000679.1:g.79767514T>C GRCh37
NG_016409.1:g.8465T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000400723.8:c.61-144T>C MANE Select ENSP00000383558.3:n.61-144T>C
ENST00000400723.7:c.61-144T>C ENSP00000383558.3:n.61-144T>C
ENST00000570996.5:c.61-144T>C ENSP00000460976.1:n.61-144T>C
ENST00000572185.1:n.356-144T>C
ENST00000573428.1:c.61-144T>C ENSP00000458930.1:n.61-144T>C
NM_000160.4:c.61-144T>C NP_000151.1:n.61-144T>C
XM_006722277.1:c.61-144T>C XP_006722340.1:n.61-144T>C
XM_011523539.1:c.-166-144T>C XP_011521841.1:n.-166-144T>C
XM_011523540.1:c.-456-144T>C XP_011521842.1:n.-456-144T>C
XM_017024446.1:c.61-150T>C XP_016879935.1:n.61-150T>C
XM_017024447.1:c.-450-150T>C XP_016879936.1:n.-450-150T>C
NM_000160.5:c.61-144T>C MANE Select NP_000151.1:n.61-144T>C
Search 100 bp 5'
Search 100 bp 3'