Canonical Allele Identifier: CA2318706338
Gene: GNA15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159675C= , CM000681.2:g.3159675C= GRCh38
NC_000019.9:g.3159673C= , CM000681.1:g.3159673C= GRCh37
NC_000019.8:g.3110673C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1794C= MANE Select ENSP00000262958.2:n.898+1794C=
ENST00000262958.3:c.898+1794C= ENSP00000262958.2:n.898+1794C=
NM_002068.3:c.898+1794C= NP_002059.3:n.898+1794C=
NM_002068.4:c.898+1794C= MANE Select NP_002059.3:n.898+1794C=
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