Canonical Allele Identifier: CA1554498
Gene: ADCY3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2632023
ClinVar RCV Id: RCV003414539
dbSNP Id: rs143034828
gnomAD v2: 2-25141368-G-C
gnomAD v3: 2-24918499-G-C
gnomAD v4: 2-24918499-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.24918499G>C , CM000664.2:g.24918499G>C GRCh38
NC_000002.11:g.25141368G>C , CM000664.1:g.25141368G>C GRCh37
NC_000002.10:g.24994872G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405392.6:c.489C>G ENSP00000384484.2:p.His163Gln
ENST00000679454.1:c.489C>G MANE Select ENSP00000505261.1:p.His163Gln
ENST00000260600.9:c.489C>G ENSP00000260600.5:p.His163Gln
ENST00000405392.5:c.489C>G ENSP00000384484.2:p.His163Gln
ENST00000435135.5:c.489C>G ENSP00000389799.1:p.His163Gln
NM_004036.3:c.489C>G NP_004027.2:p.His163Gln
XM_005264104.1:c.489C>G XP_005264161.1:p.His163Gln
XM_005264105.1:c.489C>G XP_005264162.1:p.His163Gln
XM_006711925.1:c.489C>G XP_006711988.1:p.His163Gln
XM_011532489.1:c.489C>G XP_011530791.1:p.His163Gln
XM_011532490.1:c.489C>G XP_011530792.1:p.His163Gln
XM_011532491.1:c.489C>G XP_011530793.1:p.His163Gln
XM_011532492.1:c.489C>G XP_011530794.1:p.His163Gln
XM_011532493.1:c.489C>G XP_011530795.1:p.His163Gln
XM_011532494.1:c.489C>G XP_011530796.1:p.His163Gln
NM_001320613.1:c.489C>G NP_001307542.1:p.His163Gln
NM_004036.4:c.489C>G NP_004027.2:p.His163Gln
XM_011532492.2:c.489C>G XP_011530794.1:p.His163Gln
XM_017003186.1:c.489C>G XP_016858675.1:p.His163Gln
XM_017003187.1:c.489C>G XP_016858676.1:p.His163Gln
XM_017003188.1:c.489C>G XP_016858677.1:p.His163Gln
XM_017003189.1:c.489C>G XP_016858678.1:p.His163Gln
XM_017003190.1:c.489C>G XP_016858679.1:p.His163Gln
NM_001320613.2:c.489C>G NP_001307542.1:p.His163Gln
NM_001377128.1:c.489C>G NP_001364057.1:p.His163Gln
NM_001377129.1:c.489C>G NP_001364058.1:p.His163Gln
NM_001377130.1:c.489C>G NP_001364059.1:p.His163Gln
NM_001377132.1:c.489C>G NP_001364061.1:p.His163Gln
NM_004036.5:c.489C>G MANE Select NP_004027.2:p.His163Gln