Canonical Allele Identifier: CA2318706350
Gene: GNA15 HGNC NCBI

Linked Data

dbSNP Id: rs1915103386

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159703T>G , CM000681.2:g.3159703T>G GRCh38
NC_000019.9:g.3159701T>G , CM000681.1:g.3159701T>G GRCh37
NC_000019.8:g.3110701T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1822T>G MANE Select ENSP00000262958.2:n.898+1822T>G
ENST00000262958.3:c.898+1822T>G ENSP00000262958.2:n.898+1822T>G
NM_002068.3:c.898+1822T>G NP_002059.3:n.898+1822T>G
NM_002068.4:c.898+1822T>G MANE Select NP_002059.3:n.898+1822T>G