Canonical Allele Identifier: CA2318706362
Gene: GNA15 HGNC NCBI

Linked Data

dbSNP Id: rs1915104180
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159726A>T , CM000681.2:g.3159726A>T GRCh38
NC_000019.9:g.3159724A>T , CM000681.1:g.3159724A>T GRCh37
NC_000019.8:g.3110724A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1845A>T MANE Select ENSP00000262958.2:n.898+1845A>T
ENST00000262958.3:c.898+1845A>T ENSP00000262958.2:n.898+1845A>T
NM_002068.3:c.898+1845A>T NP_002059.3:n.898+1845A>T
NM_002068.4:c.898+1845A>T MANE Select NP_002059.3:n.898+1845A>T
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