Canonical Allele Identifier: CA304315497
Gene: GNA15 HGNC NCBI

Linked Data

dbSNP Id: rs774122308
gnomAD v3: 19-3159675-C-T
gnomAD v4: 19-3159675-C-T
MyVariant Identifiers: chr19:g.3159673C>T (hg19) chr19:g.3159675C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159675C>T , CM000681.2:g.3159675C>T GRCh38
NC_000019.9:g.3159673C>T , CM000681.1:g.3159673C>T GRCh37
NC_000019.8:g.3110673C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1794C>T MANE Select ENSP00000262958.2:n.898+1794C>T
ENST00000262958.3:c.898+1794C>T ENSP00000262958.2:n.898+1794C>T
NM_002068.3:c.898+1794C>T NP_002059.3:n.898+1794C>T
NM_002068.4:c.898+1794C>T MANE Select NP_002059.3:n.898+1794C>T
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