Canonical Allele Identifier: CA992703021
Gene: GNA15 HGNC NCBI

Linked Data

dbSNP Id: rs181986661
gnomAD v3: 19-3159719-T-G
gnomAD v4: 19-3159719-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159719T>G , CM000681.2:g.3159719T>G GRCh38
NC_000019.9:g.3159717T>G , CM000681.1:g.3159717T>G GRCh37
NC_000019.8:g.3110717T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1838T>G MANE Select ENSP00000262958.2:n.898+1838T>G
ENST00000262958.3:c.898+1838T>G ENSP00000262958.2:n.898+1838T>G
NM_002068.3:c.898+1838T>G NP_002059.3:n.898+1838T>G
NM_002068.4:c.898+1838T>G MANE Select NP_002059.3:n.898+1838T>G
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