Canonical Allele Identifier: CA2318706363
Gene: GNA15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159728G= , CM000681.2:g.3159728G= GRCh38
NC_000019.9:g.3159726G= , CM000681.1:g.3159726G= GRCh37
NC_000019.8:g.3110726G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1847G= MANE Select ENSP00000262958.2:n.898+1847G=
ENST00000262958.3:c.898+1847G= ENSP00000262958.2:n.898+1847G=
NM_002068.3:c.898+1847G= NP_002059.3:n.898+1847G=
NM_002068.4:c.898+1847G= MANE Select NP_002059.3:n.898+1847G=
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