Canonical Allele Identifier: CA1047828780
Gene: GNAI2 HGNC NCBI

Linked Data

dbSNP Id: rs1700695189
gnomAD v3: 3-50256169-A-C
gnomAD v4: 3-50256169-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.50256169A>C , CM000665.2:g.50256169A>C GRCh38
NC_000003.11:g.50293601A>C , CM000665.1:g.50293601A>C GRCh37
NC_000003.10:g.50268605A>C NCBI36
NG_016002.2:g.34482A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000313601.11:c.465-23A>C MANE Select ENSP00000312999.6:n.465-23A>C
ENST00000266027.9:c.309-23A>C ENSP00000266027.6:n.309-23A>C
ENST00000313601.10:c.465-23A>C ENSP00000312999.6:n.465-23A>C
ENST00000422163.5:c.417-23A>C ENSP00000406871.1:n.417-23A>C
ENST00000440628.5:c.309-23A>C ENSP00000395736.1:n.309-23A>C
ENST00000441156.5:c.422-23A>C ENSP00000394321.1:n.422-23A>C
ENST00000446079.5:c.*100-23A>C ENSP00000406065.1:n.*100-23A>C
ENST00000451956.1:c.354-23A>C ENSP00000406369.1:n.354-23A>C
ENST00000468422.1:n.32-23A>C
ENST00000490122.5:n.1292-23A>C
ENST00000491100.5:n.2281-23A>C
NM_001166425.1:c.354-23A>C NP_001159897.1:n.354-23A>C
NM_001282617.1:c.309-23A>C NP_001269546.1:n.309-23A>C
NM_001282618.1:c.222-23A>C NP_001269547.1:n.222-23A>C
NM_001282619.1:c.417-23A>C NP_001269548.1:n.417-23A>C
NM_001282620.1:c.417-23A>C NP_001269549.1:n.417-23A>C
NM_002070.3:c.465-23A>C NP_002061.1:n.465-23A>C
NM_002070.4:c.465-23A>C MANE Select NP_002061.1:n.465-23A>C
NM_001166425.2:c.354-23A>C NP_001159897.1:n.354-23A>C
NM_001282618.2:c.222-23A>C NP_001269547.1:n.222-23A>C
NM_001282619.2:c.417-23A>C NP_001269548.1:n.417-23A>C
NM_001282620.2:c.417-23A>C NP_001269549.1:n.417-23A>C
NM_001282617.2:c.309-23A>C NP_001269546.1:n.309-23A>C