Canonical Allele Identifier: CA185369576
Gene: ADCY8 HGNC NCBI

Linked Data

dbSNP Id: rs140027471
gnomAD v2: 8-131808026-G-GGT
gnomAD v3: 8-130795780-G-GGT
gnomAD v4: 8-130795780-G-GGT
MyVariant Identifiers: chr8:g.131808032_131808033insGT (hg19) chr8:g.131808026_131808027insGT (hg19) chr8:g.130795786_130795787insGT (hg38) chr8:g.130795780_130795781insGT (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.130795797_130795798dup , CM000670.2:g.130795797_130795798dup GRCh38
NC_000008.10:g.131808043_131808044dup , CM000670.1:g.131808043_131808044dup GRCh37
NC_000008.9:g.131877225_131877226dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000286355.10:c.3060+4644_3060+4645dup MANE Select ENSP00000286355.5:n.3060+4644_3060+4645dup
ENST00000286355.9:c.3060+4644_3060+4645dup ENSP00000286355.5:n.3060+4644_3060+4645dup
ENST00000377928.7:c.2667+4644_2667+4645dup ENSP00000367161.3:n.2667+4644_2667+4645dup
NM_001115.2:c.3060+4644_3060+4645dup NP_001106.1:n.3060+4644_3060+4645dup
XM_005250769.2:c.2970+4644_2970+4645dup XP_005250826.1:n.2970+4644_2970+4645dup
XM_006716501.2:c.2862+4644_2862+4645dup XP_006716564.1:n.2862+4644_2862+4645dup
XM_005250769.3:c.2970+4644_2970+4645dup XP_005250826.1:n.2970+4644_2970+4645dup
XM_006716501.3:c.2862+4644_2862+4645dup XP_006716564.1:n.2862+4644_2862+4645dup
XM_017013006.1:c.2772+4644_2772+4645dup XP_016868495.1:n.2772+4644_2772+4645dup
NM_001115.3:c.3060+4644_3060+4645dup MANE Select NP_001106.1:n.3060+4644_3060+4645dup
Search 100 bp 5'
Search 100 bp 3'