Canonical Allele Identifier: CA2318706347
Gene: GNA15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159699A= , CM000681.2:g.3159699A= GRCh38
NC_000019.9:g.3159697A= , CM000681.1:g.3159697A= GRCh37
NC_000019.8:g.3110697A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1818A= MANE Select ENSP00000262958.2:n.898+1818A=
ENST00000262958.3:c.898+1818A= ENSP00000262958.2:n.898+1818A=
NM_002068.3:c.898+1818A= NP_002059.3:n.898+1818A=
NM_002068.4:c.898+1818A= MANE Select NP_002059.3:n.898+1818A=