Canonical Allele Identifier: CA881369707
Gene: GNA15 HGNC NCBI

Linked Data

dbSNP Id: rs574312478
gnomAD v3: 19-3159729-C-A
gnomAD v4: 19-3159729-C-A
MyVariant Identifiers: chr19:g.3159727C>A (hg19) chr19:g.3159729C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159729C>A , CM000681.2:g.3159729C>A GRCh38
NC_000019.9:g.3159727C>A , CM000681.1:g.3159727C>A GRCh37
NC_000019.8:g.3110727C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1848C>A MANE Select ENSP00000262958.2:n.898+1848C>A
ENST00000262958.3:c.898+1848C>A ENSP00000262958.2:n.898+1848C>A
NM_002068.3:c.898+1848C>A NP_002059.3:n.898+1848C>A
NM_002068.4:c.898+1848C>A MANE Select NP_002059.3:n.898+1848C>A
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