Canonical Allele Identifier: CA881369676
Gene: GNA15 HGNC NCBI

Linked Data

dbSNP Id: rs1282924320
gnomAD v3: 19-3159677-A-G
gnomAD v4: 19-3159677-A-G
MyVariant Identifiers: chr19:g.3159675A>G (hg19) chr19:g.3159677A>G (hg38)
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Genomic Alleles

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

Transcript Alleles

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