Canonical Allele Identifier: CA502298326

Gene: GCGR

Linked Data

• MyVariant Identifiers: chr17:g.79767726T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809850T>C , CM000679.2:g.81809850T>C	GRCh38
NC_000017.10:g.79767726T>C , CM000679.1:g.79767726T>C	GRCh37
NG_016409.1:g.8677T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000400723.8:c.129T>C MANE Select	ENSP00000383558.3:p.Cys43=
ENST00000400723.7:c.129T>C	ENSP00000383558.3:p.Cys43=
ENST00000570996.5:c.129T>C	ENSP00000460976.1:p.Cys43=
ENST00000572185.1:n.424T>C
ENST00000573428.1:c.129T>C	ENSP00000458930.1:p.Cys43=
ENST00000574283.2:n.63T>C
NM_000160.4:c.129T>C	NP_000151.1:p.Cys43=
XM_006722277.1:c.129T>C	XP_006722340.1:p.Cys43=
XM_011523539.1:c.-98T>C	XP_011521841.1:n.-98T>C
XM_011523540.1:c.-388T>C	XP_011521842.1:n.-388T>C
XM_017024446.1:c.123T>C	XP_016879935.1:p.Cys41=
XM_017024447.1:c.-388T>C	XP_016879936.1:n.-388T>C
NM_000160.5:c.129T>C MANE Select	NP_000151.1:p.Cys43=