Canonical Allele Identifier: CA502298357

Gene: GCGR

Linked Data

• dbSNP Id: rs2038059136
• MyVariant Identifiers: chr17:g.79767756C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809880C>T , CM000679.2:g.81809880C>T	GRCh38
NC_000017.10:g.79767756C>T , CM000679.1:g.79767756C>T	GRCh37
NG_016409.1:g.8707C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.159C>T MANE Select	ENSP00000383558.3:p.Pro53=
ENST00000400723.7:c.159C>T	ENSP00000383558.3:p.Pro53=
ENST00000570996.5:c.159C>T	ENSP00000460976.1:p.Pro53=
ENST00000572185.1:n.454C>T
ENST00000573428.1:c.159C>T	ENSP00000458930.1:p.Pro53=
ENST00000574283.2:n.93C>T
NM_000160.4:c.159C>T	NP_000151.1:p.Pro53=
XM_006722277.1:c.159C>T	XP_006722340.1:p.Pro53=
XM_011523539.1:c.-68C>T	XP_011521841.1:n.-68C>T
XM_011523540.1:c.-358C>T	XP_011521842.1:n.-358C>T
XM_017024446.1:c.153C>T	XP_016879935.1:p.Pro51=
XM_017024447.1:c.-358C>T	XP_016879936.1:n.-358C>T
NM_000160.5:c.159C>T MANE Select	NP_000151.1:p.Pro53=