Canonical Allele Identifier: CA502298338

Gene: GCGR

Linked Data

• dbSNP Id: rs1285056022
• gnomAD v3: 17-81809868-G-C
• gnomAD v4: 17-81809868-G-C
• MyVariant Identifiers: chr17:g.79767744G>C (hg19) ; chr17:g.81809868G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.81809868G>C , CM000679.2:g.81809868G>C	GRCh38
NC_000017.10:g.79767744G>C , CM000679.1:g.79767744G>C	GRCh37
NG_016409.1:g.8695G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000400723.8:c.147G>C MANE Select	ENSP00000383558.3:p.Leu49=
ENST00000400723.7:c.147G>C	ENSP00000383558.3:p.Leu49=
ENST00000570996.5:c.147G>C	ENSP00000460976.1:p.Leu49=
ENST00000572185.1:n.442G>C
ENST00000573428.1:c.147G>C	ENSP00000458930.1:p.Leu49=
ENST00000574283.2:n.81G>C
NM_000160.4:c.147G>C	NP_000151.1:p.Leu49=
XM_006722277.1:c.147G>C	XP_006722340.1:p.Leu49=
XM_011523539.1:c.-80G>C	XP_011521841.1:n.-80G>C
XM_011523540.1:c.-370G>C	XP_011521842.1:n.-370G>C
XM_017024446.1:c.141G>C	XP_016879935.1:p.Leu47=
XM_017024447.1:c.-370G>C	XP_016879936.1:n.-370G>C
NM_000160.5:c.147G>C MANE Select	NP_000151.1:p.Leu49=