Canonical Allele Identifier: CA352896108

Gene: GNAI2

Linked Data

• dbSNP Id: rs797039274
• MyVariant Identifiers: chr3:g.50293747C>G (hg19) ; chr3:g.50256315C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256315C>G , CM000665.2:g.50256315C>G	GRCh38
NC_000003.11:g.50293747C>G , CM000665.1:g.50293747C>G	GRCh37
NC_000003.10:g.50268751C>G	NCBI36
NG_016002.2:g.34628C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.588C>G MANE Select	ENSP00000312999.6:p.His196Gln
ENST00000266027.9:c.432C>G	ENSP00000266027.6:p.His144Gln
ENST00000313601.10:c.588C>G	ENSP00000312999.6:p.His196Gln
ENST00000422163.5:c.540C>G	ENSP00000406871.1:p.His180Gln
ENST00000440628.5:c.432C>G	ENSP00000395736.1:p.His144Gln
ENST00000441156.5:c.*116C>G	ENSP00000394321.1:n.*116C>G
ENST00000446079.5:c.*223C>G	ENSP00000406065.1:n.*223C>G
ENST00000451956.1:c.477C>G	ENSP00000406369.1:p.His159Gln
ENST00000468422.1:n.155C>G
ENST00000490122.5:n.1415C>G
ENST00000491100.5:n.2404C>G
ENST00000492383.1:n.33C>G
NM_001166425.1:c.477C>G	NP_001159897.1:p.His159Gln
NM_001282617.1:c.432C>G	NP_001269546.1:p.His144Gln
NM_001282618.1:c.345C>G	NP_001269547.1:p.His115Gln
NM_001282619.1:c.540C>G	NP_001269548.1:p.His180Gln
NM_001282620.1:c.540C>G	NP_001269549.1:p.His180Gln
NM_002070.3:c.588C>G	NP_002061.1:p.His196Gln
NM_002070.4:c.588C>G MANE Select	NP_002061.1:p.His196Gln
NM_001166425.2:c.477C>G	NP_001159897.1:p.His159Gln
NM_001282618.2:c.345C>G	NP_001269547.1:p.His115Gln
NM_001282619.2:c.540C>G	NP_001269548.1:p.His180Gln
NM_001282620.2:c.540C>G	NP_001269549.1:p.His180Gln
NM_001282617.2:c.432C>G	NP_001269546.1:p.His144Gln