Canonical Allele Identifier: CA502298347

Gene: GCGR

Linked Data

• MyVariant Identifiers: chr17:g.79767750C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809874C>G , CM000679.2:g.81809874C>G	GRCh38
NC_000017.10:g.79767750C>G , CM000679.1:g.79767750C>G	GRCh37
NG_016409.1:g.8701C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.153C>G MANE Select	ENSP00000383558.3:p.Pro51=
ENST00000400723.7:c.153C>G	ENSP00000383558.3:p.Pro51=
ENST00000570996.5:c.153C>G	ENSP00000460976.1:p.Pro51=
ENST00000572185.1:n.448C>G
ENST00000573428.1:c.153C>G	ENSP00000458930.1:p.Pro51=
ENST00000574283.2:n.87C>G
NM_000160.4:c.153C>G	NP_000151.1:p.Pro51=
XM_006722277.1:c.153C>G	XP_006722340.1:p.Pro51=
XM_011523539.1:c.-74C>G	XP_011521841.1:n.-74C>G
XM_011523540.1:c.-364C>G	XP_011521842.1:n.-364C>G
XM_017024446.1:c.147C>G	XP_016879935.1:p.Pro49=
XM_017024447.1:c.-364C>G	XP_016879936.1:n.-364C>G
NM_000160.5:c.153C>G MANE Select	NP_000151.1:p.Pro51=