Canonical Allele Identifier: CA1149119407

Gene: GNB1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1804624A= , CM000663.2:g.1804624A=	GRCh38
NC_000001.10:g.1736063A= , CM000663.1:g.1736063A=	GRCh37
NC_000001.9:g.1725923A=	NCBI36
NG_047052.1:g.91494T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000439272.7:c.229-43T=	ENSP00000399741.3:n.229-43T=
ENST00000615252.5:c.-33-43T=	ENSP00000483532.1:n.-33-43T=
ENST00000703692.1:c.268-43T=	ENSP00000515427.1:n.268-43T=
ENST00000703693.1:c.268-43T=	ENSP00000515428.1:n.268-43T=
ENST00000703694.1:c.268-43T=	ENSP00000515429.1:n.268-43T=
ENST00000703695.1:c.268-43T=	ENSP00000515430.1:n.268-43T=
ENST00000703696.1:c.268-43T=	ENSP00000515431.1:n.268-43T=
ENST00000703697.1:c.268-43T=	ENSP00000515432.1:n.268-43T=
ENST00000703699.1:c.268-43T=	ENSP00000515433.1:n.268-43T=
ENST00000703700.1:c.268-43T=	ENSP00000515434.1:n.268-43T=
ENST00000703701.1:c.268-43T=	ENSP00000515435.1:n.268-43T=
ENST00000703702.1:c.268-43T=	ENSP00000515436.1:n.268-43T=
ENST00000703703.1:c.268-43T=	ENSP00000515437.1:n.268-43T=
ENST00000703704.1:c.268-43T=	ENSP00000515438.1:n.268-43T=
ENST00000703705.1:c.136-43T=	ENSP00000515439.1:n.136-43T=
ENST00000703706.1:c.268-43T=	ENSP00000515440.1:n.268-43T=
ENST00000703707.1:c.229-43T=	ENSP00000515441.1:n.229-43T=
ENST00000703708.1:c.268-43T=	ENSP00000515442.1:n.268-43T=
ENST00000703709.1:c.268-43T=	ENSP00000515443.1:n.268-43T=
ENST00000703710.1:c.268-43T=	ENSP00000515444.1:n.268-43T=
ENST00000703711.1:c.268-43T=	ENSP00000515445.1:n.268-43T=
ENST00000378609.9:c.268-43T= MANE Select	ENSP00000367872.3:n.268-43T=
ENST00000378609.8:c.268-43T=	ENSP00000367872.3:n.268-43T=
ENST00000434686.6:c.268-43T=	ENSP00000392765.2:n.268-43T=
ENST00000437146.1:c.268-43T=	ENSP00000416651.1:n.268-43T=
ENST00000439272.6:c.229-43T=	ENSP00000399741.2:n.229-43T=
ENST00000471354.1:n.872-43T=
ENST00000610897.4:c.268-43T=	ENSP00000481878.1:n.268-43T=
ENST00000615252.4:c.-33-43T=	ENSP00000483532.1:n.-33-43T=
NM_001282538.1:c.-33-43T=	NP_001269467.1:n.-33-43T=
NM_001282539.1:c.268-43T=	NP_001269468.1:n.268-43T=
NM_002074.4:c.268-43T=	NP_002065.1:n.268-43T=
XM_017001059.2:c.268-43T=	XP_016856548.1:n.268-43T=
XM_017001060.2:c.268-43T=	XP_016856549.1:n.268-43T=
XM_017001061.2:c.268-43T=	XP_016856550.1:n.268-43T=
XM_024446495.1:c.268-43T=	XP_024302263.1:n.268-43T=
NM_002074.5:c.268-43T= MANE Select	NP_002065.1:n.268-43T=
NM_001282538.2:c.-33-43T=	NP_001269467.1:n.-33-43T=
NM_001282539.2:c.268-43T=	NP_001269468.1:n.268-43T=