Canonical Allele Identifier: CA631491246
Gene: GNA15 HGNC NCBI

Linked Data

dbSNP Id: rs1325902626
gnomAD v2: 19-3159697-A-T
gnomAD v3: 19-3159699-A-T
gnomAD v4: 19-3159699-A-T
MyVariant Identifiers: chr19:g.3159697A>T (hg19) chr19:g.3159699A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159699A>T , CM000681.2:g.3159699A>T GRCh38
NC_000019.9:g.3159697A>T , CM000681.1:g.3159697A>T GRCh37
NC_000019.8:g.3110697A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1818A>T MANE Select ENSP00000262958.2:n.898+1818A>T
ENST00000262958.3:c.898+1818A>T ENSP00000262958.2:n.898+1818A>T
NM_002068.3:c.898+1818A>T NP_002059.3:n.898+1818A>T
NM_002068.4:c.898+1818A>T MANE Select NP_002059.3:n.898+1818A>T
Search 100 bp 5'
Search 100 bp 3'