Canonical Allele Identifier: CA881369698
Gene: GNA15 HGNC NCBI

Linked Data

dbSNP Id: rs1479247089
gnomAD v3: 19-3159721-CT-C
gnomAD v4: 19-3159721-CT-C
MyVariant Identifiers: chr19:g.3159720del (hg19) chr19:g.3159722del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.3159724del , CM000681.2:g.3159724del GRCh38
NC_000019.9:g.3159722del , CM000681.1:g.3159722del GRCh37
NC_000019.8:g.3110722del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262958.4:c.898+1843del MANE Select ENSP00000262958.2:n.898+1843del
ENST00000262958.3:c.898+1843del ENSP00000262958.2:n.898+1843del
NM_002068.3:c.898+1843del NP_002059.3:n.898+1843del
NM_002068.4:c.898+1843del MANE Select NP_002059.3:n.898+1843del
Search 100 bp 5'
Search 100 bp 3'