Canonical Allele Identifier: CA433695325

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293693C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256261C>G , CM000665.2:g.50256261C>G	GRCh38
NC_000003.11:g.50293693C>G , CM000665.1:g.50293693C>G	GRCh37
NC_000003.10:g.50268697C>G	NCBI36
NG_016002.2:g.34574C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.534C>G MANE Select	ENSP00000312999.6:p.Thr178=
ENST00000266027.9:c.378C>G	ENSP00000266027.6:p.Thr126=
ENST00000313601.10:c.534C>G	ENSP00000312999.6:p.Thr178=
ENST00000422163.5:c.486C>G	ENSP00000406871.1:p.Thr162=
ENST00000440628.5:c.378C>G	ENSP00000395736.1:p.Thr126=
ENST00000441156.5:c.*62C>G	ENSP00000394321.1:n.*62C>G
ENST00000446079.5:c.*169C>G	ENSP00000406065.1:n.*169C>G
ENST00000451956.1:c.423C>G	ENSP00000406369.1:p.Thr141=
ENST00000468422.1:n.101C>G
ENST00000490122.5:n.1361C>G
ENST00000491100.5:n.2350C>G
NM_001166425.1:c.423C>G	NP_001159897.1:p.Thr141=
NM_001282617.1:c.378C>G	NP_001269546.1:p.Thr126=
NM_001282618.1:c.291C>G	NP_001269547.1:p.Thr97=
NM_001282619.1:c.486C>G	NP_001269548.1:p.Thr162=
NM_001282620.1:c.486C>G	NP_001269549.1:p.Thr162=
NM_002070.3:c.534C>G	NP_002061.1:p.Thr178=
NM_002070.4:c.534C>G MANE Select	NP_002061.1:p.Thr178=
NM_001166425.2:c.423C>G	NP_001159897.1:p.Thr141=
NM_001282618.2:c.291C>G	NP_001269547.1:p.Thr97=
NM_001282619.2:c.486C>G	NP_001269548.1:p.Thr162=
NM_001282620.2:c.486C>G	NP_001269549.1:p.Thr162=
NM_001282617.2:c.378C>G	NP_001269546.1:p.Thr126=