Canonical Allele Identifier: CA992703010
Gene: GNA15 HGNC NCBI

Linked Data

dbSNP Id: rs1915103420
gnomAD v3: 19-3159704-T-C
gnomAD v4: 19-3159704-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159704T>C , CM000681.2:g.3159704T>C GRCh38
NC_000019.9:g.3159702T>C , CM000681.1:g.3159702T>C GRCh37
NC_000019.8:g.3110702T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1823T>C MANE Select ENSP00000262958.2:n.898+1823T>C
ENST00000262958.3:c.898+1823T>C ENSP00000262958.2:n.898+1823T>C
NM_002068.3:c.898+1823T>C NP_002059.3:n.898+1823T>C
NM_002068.4:c.898+1823T>C MANE Select NP_002059.3:n.898+1823T>C
Search 100 bp 5'
Search 100 bp 3'