Canonical Allele Identifier: CA11060778
Gene: ADCY3 HGNC NCBI

Linked Data

dbSNP Id: rs13407913

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24874775A>G , CM000664.2:g.24874775A>G GRCh38
NC_000002.11:g.25097644A>G , CM000664.1:g.25097644A>G GRCh37
NC_000002.10:g.24951148A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000260600.9:c.676-2056T>C ENSP00000260600.5:p.=
ENST00000405392.5:c.676-2056T>C ENSP00000384484.2:p.=
ENST00000433852.1:c.10-2056T>C ENSP00000401455.1:p.=
ENST00000435135.5:c.676-32391T>C ENSP00000389799.1:p.=
NM_004036.3:c.676-2056T>C NP_004027.2:p.=
XM_005264104.1:c.676-2056T>C XP_005264161.1:p.=
XM_005264105.1:c.676-2056T>C XP_005264162.1:p.=
XM_006711925.1:c.676-2056T>C XP_006711988.1:p.=
XM_011532489.1:c.676-2056T>C XP_011530791.1:p.=
XM_011532490.1:c.676-2056T>C XP_011530792.1:p.=
XM_011532491.1:c.676-2056T>C XP_011530793.1:p.=
XM_011532492.1:c.676-2056T>C XP_011530794.1:p.=
XM_011532493.1:c.676-2056T>C XP_011530795.1:p.=
XM_011532494.1:c.676-2056T>C XP_011530796.1:p.=
XM_011532495.1:c.10-2056T>C XP_011530797.1:p.=
XM_011532496.1:c.-48-2056T>C XP_011530798.1:p.=
NM_001320613.1:c.676-2056T>C NP_001307542.1:p.=
NM_004036.4:c.676-2056T>C NP_004027.2:p.=
XM_011532492.2:c.676-2056T>C XP_011530794.1:p.=
XM_017003186.1:c.676-2056T>C XP_016858675.1:p.=
XM_017003187.1:c.676-2056T>C XP_016858676.1:p.=
XM_017003188.1:c.676-2056T>C XP_016858677.1:p.=
XM_017003189.1:c.676-2056T>C XP_016858678.1:p.=
XM_017003190.1:c.676-2056T>C XP_016858679.1:p.=
XM_017003191.1:c.40-2056T>C XP_016858680.1:p.=
XM_017003192.1:c.-48-2056T>C XP_016858681.1:p.=
XM_017003193.1:c.-48-2056T>C XP_016858682.1:p.=
NM_001320613.2:c.676-2056T>C NP_001307542.1:p.=
NM_001377128.1:c.676-2056T>C NP_001364057.1:p.=
NM_001377129.1:c.676-2056T>C NP_001364058.1:p.=
NM_001377130.1:c.676-2056T>C NP_001364059.1:p.=
NM_001377131.1:c.-48-2056T>C NP_001364060.1:p.=
NM_001377132.1:c.676-2056T>C NP_001364061.1:p.=
NM_004036.5:c.676-2056T>C MANE Select NP_004027.2:p.=