Canonical Allele Identifier: CA433694575

Gene: GNAI2

Linked Data

• gnomAD v4: 3-50256192-C-T
• MyVariant Identifiers: chr3:g.50293624C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256192C>T , CM000665.2:g.50256192C>T	GRCh38
NC_000003.11:g.50293624C>T , CM000665.1:g.50293624C>T	GRCh37
NC_000003.10:g.50268628C>T	NCBI36
NG_016002.2:g.34505C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.465C>T MANE Select	ENSP00000312999.6:p.Tyr155=
ENST00000266027.9:c.309C>T	ENSP00000266027.6:p.Tyr103=
ENST00000313601.10:c.465C>T	ENSP00000312999.6:p.Tyr155=
ENST00000422163.5:c.417C>T	ENSP00000406871.1:p.Tyr139=
ENST00000440628.5:c.309C>T	ENSP00000395736.1:p.Tyr103=
ENST00000441156.5:c.422C>T	ENSP00000394321.1:p.Thr141Ile
ENST00000446079.5:c.*100C>T	ENSP00000406065.1:n.*100C>T
ENST00000451956.1:c.354C>T	ENSP00000406369.1:p.Tyr118=
ENST00000468422.1:n.32C>T
ENST00000490122.5:n.1292C>T
ENST00000491100.5:n.2281C>T
NM_001166425.1:c.354C>T	NP_001159897.1:p.Tyr118=
NM_001282617.1:c.309C>T	NP_001269546.1:p.Tyr103=
NM_001282618.1:c.222C>T	NP_001269547.1:p.Tyr74=
NM_001282619.1:c.417C>T	NP_001269548.1:p.Tyr139=
NM_001282620.1:c.417C>T	NP_001269549.1:p.Tyr139=
NM_002070.3:c.465C>T	NP_002061.1:p.Tyr155=
NM_002070.4:c.465C>T MANE Select	NP_002061.1:p.Tyr155=
NM_001166425.2:c.354C>T	NP_001159897.1:p.Tyr118=
NM_001282618.2:c.222C>T	NP_001269547.1:p.Tyr74=
NM_001282619.2:c.417C>T	NP_001269548.1:p.Tyr139=
NM_001282620.2:c.417C>T	NP_001269549.1:p.Tyr139=
NM_001282617.2:c.309C>T	NP_001269546.1:p.Tyr103=