Canonical Allele Identifier: CA352895368

Gene: GNAI2

Linked Data

• MyVariant Identifiers: chr3:g.50293675G>C (hg19) ; chr3:g.50256243G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.50256243G>C , CM000665.2:g.50256243G>C	GRCh38
NC_000003.11:g.50293675G>C , CM000665.1:g.50293675G>C	GRCh37
NC_000003.10:g.50268679G>C	NCBI36
NG_016002.2:g.34556G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313601.11:c.516G>C MANE Select	ENSP00000312999.6:p.Gln172His
ENST00000266027.9:c.360G>C	ENSP00000266027.6:p.Gln120His
ENST00000313601.10:c.516G>C	ENSP00000312999.6:p.Gln172His
ENST00000422163.5:c.468G>C	ENSP00000406871.1:p.Gln156His
ENST00000440628.5:c.360G>C	ENSP00000395736.1:p.Gln120His
ENST00000441156.5:c.*44G>C	ENSP00000394321.1:n.*44G>C
ENST00000446079.5:c.*151G>C	ENSP00000406065.1:n.*151G>C
ENST00000451956.1:c.405G>C	ENSP00000406369.1:p.Gln135His
ENST00000468422.1:n.83G>C
ENST00000490122.5:n.1343G>C
ENST00000491100.5:n.2332G>C
NM_001166425.1:c.405G>C	NP_001159897.1:p.Gln135His
NM_001282617.1:c.360G>C	NP_001269546.1:p.Gln120His
NM_001282618.1:c.273G>C	NP_001269547.1:p.Gln91His
NM_001282619.1:c.468G>C	NP_001269548.1:p.Gln156His
NM_001282620.1:c.468G>C	NP_001269549.1:p.Gln156His
NM_002070.3:c.516G>C	NP_002061.1:p.Gln172His
NM_002070.4:c.516G>C MANE Select	NP_002061.1:p.Gln172His
NM_001166425.2:c.405G>C	NP_001159897.1:p.Gln135His
NM_001282618.2:c.273G>C	NP_001269547.1:p.Gln91His
NM_001282619.2:c.468G>C	NP_001269548.1:p.Gln156His
NM_001282620.2:c.468G>C	NP_001269549.1:p.Gln156His
NM_001282617.2:c.360G>C	NP_001269546.1:p.Gln120His