Canonical Allele Identifier: CA813935666
Gene: ADCY2 HGNC NCBI

Linked Data

dbSNP Id: rs1269277164
gnomAD v3: 5-7517176-CT-C
gnomAD v4: 5-7517176-CT-C

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7517180del , CM000667.2:g.7517180del GRCh38
NC_000005.9:g.7517293del , CM000667.1:g.7517293del GRCh37
NC_000005.8:g.7570293del NCBI36
NG_046913.1:g.125951del

Transcript Alleles

HGVS Amino-acid change
ENST00000338316.9:c.409-3558del MANE Select ENSP00000342952.4:n.409-3558del
ENST00000338316.8:c.409-3558del ENSP00000342952.4:n.409-3558del
ENST00000484965.5:n.143-3558del
ENST00000498598.1:n.108-3558del
ENST00000537121.5:c.409-3558del ENSP00000444803.2:n.409-3558del
NM_020546.2:c.409-3558del NP_065433.2:n.409-3558del
XM_011513942.1:c.409-3558del XP_011512244.1:n.409-3558del
XR_427657.2:n.423-3558del
XM_011513942.2:c.409-3558del XP_011512244.1:n.409-3558del
XR_001741973.1:n.423-3558del
XR_001741974.2:n.423-3558del
NM_020546.3:c.409-3558del MANE Select NP_065433.2:n.409-3558del