Canonical Allele Identifier: CA11110899
Gene: ADCY3 HGNC NCBI

Linked Data

dbSNP Id: rs753529

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24831392G>A , CM000664.2:g.24831392G>A GRCh38
NC_000002.11:g.25054261G>A , CM000664.1:g.25054261G>A GRCh37
NC_000002.10:g.24907765G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260600.9:c.2055+270C>T ENSP00000260600.5:p.=
ENST00000405392.5:c.2055+270C>T ENSP00000384484.2:p.=
ENST00000455323.1:n.72+270C>T ENSP00000402008.1:p.=
ENST00000606682.5:n.1134+270C>T ENSP00000475652.1:p.=
NM_004036.3:c.2055+270C>T NP_004027.2:p.=
XM_005264104.1:c.2055+270C>T XP_005264161.1:p.=
XM_005264105.1:c.2055+270C>T XP_005264162.1:p.=
XM_006711925.1:c.2121+270C>T XP_006711988.1:p.=
XM_011532489.1:c.2178+270C>T XP_011530791.1:p.=
XM_011532490.1:c.2178+270C>T XP_011530792.1:p.=
XM_011532491.1:c.2112+270C>T XP_011530793.1:p.=
XM_011532492.1:c.2178+270C>T XP_011530794.1:p.=
XM_011532493.1:c.2178+270C>T XP_011530795.1:p.=
XM_011532494.1:c.2121+270C>T XP_011530796.1:p.=
XM_011532495.1:c.1512+270C>T XP_011530797.1:p.=
XM_011532496.1:c.1455+270C>T XP_011530798.1:p.=
NM_001320613.1:c.2055+270C>T NP_001307542.1:p.=
NM_004036.4:c.2055+270C>T NP_004027.2:p.=
XM_011532492.2:c.2178+270C>T XP_011530794.1:p.=
XM_017003186.1:c.2121+270C>T XP_016858675.1:p.=
XM_017003187.1:c.2112+270C>T XP_016858676.1:p.=
XM_017003188.1:c.2178+270C>T XP_016858677.1:p.=
XM_017003189.1:c.2178+270C>T XP_016858678.1:p.=
XM_017003190.1:c.2055+270C>T XP_016858679.1:p.=
XM_017003191.1:c.1542+270C>T XP_016858680.1:p.=
XM_017003192.1:c.1332+270C>T XP_016858681.1:p.=
XM_017003193.1:c.1332+270C>T XP_016858682.1:p.=
NM_001320613.2:c.2055+270C>T NP_001307542.1:p.=
NM_001377128.1:c.2121+270C>T NP_001364057.1:p.=
NM_001377129.1:c.2055+270C>T NP_001364058.1:p.=
NM_001377130.1:c.2055+270C>T NP_001364059.1:p.=
NM_001377131.1:c.1332+270C>T NP_001364060.1:p.=
NM_001377132.1:c.2055+270C>T NP_001364061.1:p.=
NM_004036.5:c.2055+270C>T MANE Select NP_004027.2:p.=