Canonical Allele Identifier: CA14631732
Gene: GNA15 HGNC NCBI

Linked Data

dbSNP Id: rs11880825
gnomAD v2: 19-3159712-T-C
gnomAD v3: 19-3159714-T-C
gnomAD v4: 19-3159714-T-C
MyVariant Identifiers: chr19:g.3159712T>C (hg19) chr19:g.3159714T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159714T>C , CM000681.2:g.3159714T>C GRCh38
NC_000019.9:g.3159712T>C , CM000681.1:g.3159712T>C GRCh37
NC_000019.8:g.3110712T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1833T>C MANE Select ENSP00000262958.2:n.898+1833T>C
ENST00000262958.3:c.898+1833T>C ENSP00000262958.2:n.898+1833T>C
NM_002068.3:c.898+1833T>C NP_002059.3:n.898+1833T>C
NM_002068.4:c.898+1833T>C MANE Select NP_002059.3:n.898+1833T>C
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