Canonical Allele Identifier: CA2318706346
Gene: GNA15 HGNC NCBI

Linked Data

dbSNP Id: rs1915103247

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159698T>G , CM000681.2:g.3159698T>G GRCh38
NC_000019.9:g.3159696T>G , CM000681.1:g.3159696T>G GRCh37
NC_000019.8:g.3110696T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1817T>G MANE Select ENSP00000262958.2:n.898+1817T>G
ENST00000262958.3:c.898+1817T>G ENSP00000262958.2:n.898+1817T>G
NM_002068.3:c.898+1817T>G NP_002059.3:n.898+1817T>G
NM_002068.4:c.898+1817T>G MANE Select NP_002059.3:n.898+1817T>G