Canonical Allele Identifier: CA304315503
Gene: GNA15 HGNC NCBI

Linked Data

dbSNP Id: rs941326577
gnomAD v3: 19-3159694-A-C
gnomAD v4: 19-3159694-A-C
MyVariant Identifiers: chr19:g.3159692A>C (hg19) chr19:g.3159694A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159694A>C , CM000681.2:g.3159694A>C GRCh38
NC_000019.9:g.3159692A>C , CM000681.1:g.3159692A>C GRCh37
NC_000019.8:g.3110692A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1813A>C MANE Select ENSP00000262958.2:n.898+1813A>C
ENST00000262958.3:c.898+1813A>C ENSP00000262958.2:n.898+1813A>C
NM_002068.3:c.898+1813A>C NP_002059.3:n.898+1813A>C
NM_002068.4:c.898+1813A>C MANE Select NP_002059.3:n.898+1813A>C
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