Canonical Allele Identifier: CA2318706339
Gene: GNA15 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159677A= , CM000681.2:g.3159677A= GRCh38
NC_000019.9:g.3159675A= , CM000681.1:g.3159675A= GRCh37
NC_000019.8:g.3110675A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1796A= MANE Select ENSP00000262958.2:n.898+1796A=
ENST00000262958.3:c.898+1796A= ENSP00000262958.2:n.898+1796A=
NM_002068.3:c.898+1796A= NP_002059.3:n.898+1796A=
NM_002068.4:c.898+1796A= MANE Select NP_002059.3:n.898+1796A=
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