Canonical Allele Identifier: CA304315537
Gene: GNA15 HGNC NCBI

Linked Data

dbSNP Id: rs137878789
gnomAD v2: 19-3159782-G-C
gnomAD v3: 19-3159784-G-C
gnomAD v4: 19-3159784-G-C
MyVariant Identifiers: chr19:g.3159782G>C (hg19) chr19:g.3159784G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159784G>C , CM000681.2:g.3159784G>C GRCh38
NC_000019.9:g.3159782G>C , CM000681.1:g.3159782G>C GRCh37
NC_000019.8:g.3110782G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262958.4:c.898+1903G>C MANE Select ENSP00000262958.2:n.898+1903G>C
ENST00000262958.3:c.898+1903G>C ENSP00000262958.2:n.898+1903G>C
NM_002068.3:c.898+1903G>C NP_002059.3:n.898+1903G>C
NM_002068.4:c.898+1903G>C MANE Select NP_002059.3:n.898+1903G>C
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