Canonical Allele Identifier: CA437178060

Gene: GNB4

Linked Data

• gnomAD v4: 3-179420892-A-G
• MyVariant Identifiers: chr3:g.179138680A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.179420892A>G , CM000665.2:g.179420892A>G	GRCh38
NC_000003.11:g.179138680A>G , CM000665.1:g.179138680A>G	GRCh37
NC_000003.10:g.180621374A>G	NCBI36
NG_033163.1:g.35692T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000232564.8:c.93T>C MANE Select	ENSP00000232564.3:p.Val31=
ENST00000465153.2:c.93T>C	ENSP00000502010.1:p.Val31=
ENST00000466899.6:c.93T>C	ENSP00000420066.2:p.Val31=
ENST00000468623.6:c.58-1387T>C	ENSP00000419693.2:n.58-1387T>C
ENST00000674713.1:c.-16T>C	ENSP00000502144.1:n.-16T>C
ENST00000674862.1:c.93T>C	ENSP00000502628.1:p.Val31=
ENST00000674927.1:c.93T>C	ENSP00000501774.1:p.Val31=
ENST00000675901.1:c.93T>C	ENSP00000501992.1:p.Val31=
ENST00000676128.1:c.93T>C	ENSP00000501882.1:p.Val31=
ENST00000232564.7:c.93T>C	ENSP00000232564.3:p.Val31=
ENST00000468623.5:c.93T>C	ENSP00000419693.1:p.Val31=
ENST00000497513.1:c.93T>C	ENSP00000420606.1:p.Val31=
NM_021629.3:c.93T>C	NP_067642.1:p.Val31=
XM_005247692.1:c.93T>C	XP_005247749.1:p.Val31=
XM_006713721.1:c.93T>C	XP_006713784.1:p.Val31=
XM_011513061.1:c.93T>C	XP_011511363.1:p.Val31=
XM_005247692.2:c.93T>C	XP_005247749.1:p.Val31=
XM_006713721.2:c.93T>C	XP_006713784.1:p.Val31=
NM_021629.4:c.93T>C MANE Select	NP_067642.1:p.Val31=