Canonical Allele Identifier: CA433695398

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293705C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256273C>T , CM000665.2:g.50256273C>T	GRCh38
NC_000003.11:g.50293705C>T , CM000665.1:g.50293705C>T	GRCh37
NC_000003.10:g.50268709C>T	NCBI36
NG_016002.2:g.34586C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000313601.11:c.546C>T MANE Select	ENSP00000312999.6:p.Thr182=
ENST00000266027.9:c.390C>T	ENSP00000266027.6:p.Thr130=
ENST00000313601.10:c.546C>T	ENSP00000312999.6:p.Thr182=
ENST00000422163.5:c.498C>T	ENSP00000406871.1:p.Thr166=
ENST00000440628.5:c.390C>T	ENSP00000395736.1:p.Thr130=
ENST00000441156.5:c.*74C>T	ENSP00000394321.1:n.*74C>T
ENST00000446079.5:c.*181C>T	ENSP00000406065.1:n.*181C>T
ENST00000451956.1:c.435C>T	ENSP00000406369.1:p.Thr145=
ENST00000468422.1:n.113C>T
ENST00000490122.5:n.1373C>T
ENST00000491100.5:n.2362C>T
NM_001166425.1:c.435C>T	NP_001159897.1:p.Thr145=
NM_001282617.1:c.390C>T	NP_001269546.1:p.Thr130=
NM_001282618.1:c.303C>T	NP_001269547.1:p.Thr101=
NM_001282619.1:c.498C>T	NP_001269548.1:p.Thr166=
NM_001282620.1:c.498C>T	NP_001269549.1:p.Thr166=
NM_002070.3:c.546C>T	NP_002061.1:p.Thr182=
NM_002070.4:c.546C>T MANE Select	NP_002061.1:p.Thr182=
NM_001166425.2:c.435C>T	NP_001159897.1:p.Thr145=
NM_001282618.2:c.303C>T	NP_001269547.1:p.Thr101=
NM_001282619.2:c.498C>T	NP_001269548.1:p.Thr166=
NM_001282620.2:c.498C>T	NP_001269549.1:p.Thr166=
NM_001282617.2:c.390C>T	NP_001269546.1:p.Thr130=