Canonical Allele Identifier: CA352894762
Gene: GNAI2 HGNC NCBI

Linked Data

gnomAD v4: 3-50256195-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50256195C>A , CM000665.2:g.50256195C>A GRCh38
NC_000003.11:g.50293627C>A , CM000665.1:g.50293627C>A GRCh37
NC_000003.10:g.50268631C>A NCBI36
NG_016002.2:g.34508C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313601.11:c.468C>A MANE Select ENSP00000312999.6:p.Tyr156Ter
ENST00000266027.9:c.312C>A ENSP00000266027.6:p.Tyr104Ter
ENST00000313601.10:c.468C>A ENSP00000312999.6:p.Tyr156Ter
ENST00000422163.5:c.420C>A ENSP00000406871.1:p.Tyr140Ter
ENST00000440628.5:c.312C>A ENSP00000395736.1:p.Tyr104Ter
ENST00000441156.5:c.425C>A ENSP00000394321.1:p.Thr142Asn
ENST00000446079.5:c.*103C>A ENSP00000406065.1:n.*103C>A
ENST00000451956.1:c.357C>A ENSP00000406369.1:p.Tyr119Ter
ENST00000468422.1:n.35C>A
ENST00000490122.5:n.1295C>A
ENST00000491100.5:n.2284C>A
NM_001166425.1:c.357C>A NP_001159897.1:p.Tyr119Ter
NM_001282617.1:c.312C>A NP_001269546.1:p.Tyr104Ter
NM_001282618.1:c.225C>A NP_001269547.1:p.Tyr75Ter
NM_001282619.1:c.420C>A NP_001269548.1:p.Tyr140Ter
NM_001282620.1:c.420C>A NP_001269549.1:p.Tyr140Ter
NM_002070.3:c.468C>A NP_002061.1:p.Tyr156Ter
NM_002070.4:c.468C>A MANE Select NP_002061.1:p.Tyr156Ter
NM_001166425.2:c.357C>A NP_001159897.1:p.Tyr119Ter
NM_001282618.2:c.225C>A NP_001269547.1:p.Tyr75Ter
NM_001282619.2:c.420C>A NP_001269548.1:p.Tyr140Ter
NM_001282620.2:c.420C>A NP_001269549.1:p.Tyr140Ter
NM_001282617.2:c.312C>A NP_001269546.1:p.Tyr104Ter