Canonical Allele Identifier: CA2735466668
Gene: GNA15 HGNC NCBI

Linked Data

dbSNP Id: rs2144864119
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159692A>G , CM000681.2:g.3159692A>G GRCh38
NC_000019.9:g.3159690A>G , CM000681.1:g.3159690A>G GRCh37
NC_000019.8:g.3110690A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1811A>G MANE Select ENSP00000262958.2:n.898+1811A>G
ENST00000262958.3:c.898+1811A>G ENSP00000262958.2:n.898+1811A>G
NM_002068.3:c.898+1811A>G NP_002059.3:n.898+1811A>G
NM_002068.4:c.898+1811A>G MANE Select NP_002059.3:n.898+1811A>G
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