Canonical Allele Identifier: CA657201092

Gene: GNA15

Linked Data

• COSMIC: COSN9354193

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.3159687A>G , CM000681.2:g.3159687A>G	GRCh38
NC_000019.9:g.3159685A>G , CM000681.1:g.3159685A>G	GRCh37
NC_000019.8:g.3110685A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262958.4:c.898+1806A>G MANE Select	ENSP00000262958.2:n.898+1806A>G
ENST00000262958.3:c.898+1806A>G	ENSP00000262958.2:n.898+1806A>G
NM_002068.3:c.898+1806A>G	NP_002059.3:n.898+1806A>G
NM_002068.4:c.898+1806A>G MANE Select	NP_002059.3:n.898+1806A>G