Canonical Allele Identifier: CA304315513
Gene: GNA15 HGNC NCBI

Linked Data

dbSNP Id: rs752099185
gnomAD v2: 19-3159715-CCTT-C
gnomAD v3: 19-3159717-CCTT-C
gnomAD v4: 19-3159717-CCTT-C
MyVariant Identifiers: chr19:g.3159716_3159718del (hg19) chr19:g.3159718_3159720del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159721_3159723del , CM000681.2:g.3159721_3159723del GRCh38
NC_000019.9:g.3159719_3159721del , CM000681.1:g.3159719_3159721del GRCh37
NC_000019.8:g.3110719_3110721del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1840_898+1842del MANE Select ENSP00000262958.2:n.898+1840_898+1842del
ENST00000262958.3:c.898+1840_898+1842del ENSP00000262958.2:n.898+1840_898+1842del
NM_002068.3:c.898+1840_898+1842del NP_002059.3:n.898+1840_898+1842del
NM_002068.4:c.898+1840_898+1842del MANE Select NP_002059.3:n.898+1840_898+1842del
Search 100 bp 5'
Search 100 bp 3'