Canonical Allele Identifier: CA346062887

Gene: ADCY3

Linked Data

• dbSNP Id: rs1668056943
• gnomAD v3: 2-24823300-T-C
• gnomAD v4: 2-24823300-T-C
• MyVariant Identifiers: chr2:g.25046169T>C (hg19) ; chr2:g.24823300T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823300T>C , CM000664.2:g.24823300T>C	GRCh38
NC_000002.11:g.25046169T>C , CM000664.1:g.25046169T>C	GRCh37
NC_000002.10:g.24899673T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2795A>G	ENSP00000384484.2:p.Asn932Ser
ENST00000679454.1:c.2792A>G MANE Select	ENSP00000505261.1:p.Asn931Ser
ENST00000260600.9:c.2792A>G	ENSP00000260600.5:p.Asn931Ser
ENST00000405392.5:c.2795A>G	ENSP00000384484.2:p.Asn932Ser
ENST00000485887.1:n.64A>G
ENST00000606682.5:c.1733A>G	ENSP00000475652.1:p.Asn578Ser
NM_004036.3:c.2792A>G	NP_004027.2:p.Asn931Ser
XM_005264104.1:c.2795A>G	XP_005264161.1:p.Asn932Ser
XM_005264105.1:c.2792A>G	XP_005264162.1:p.Asn931Ser
XM_006711925.1:c.2861A>G	XP_006711988.1:p.Asn954Ser
XM_011532489.1:c.2918A>G	XP_011530791.1:p.Asn973Ser
XM_011532490.1:c.2915A>G	XP_011530792.1:p.Asn972Ser
XM_011532491.1:c.2852A>G	XP_011530793.1:p.Asn951Ser
XM_011532492.1:c.2918A>G	XP_011530794.1:p.Asn973Ser
XM_011532493.1:c.2780A>G	XP_011530795.1:p.Asn927Ser
XM_011532494.1:c.2720A>G	XP_011530796.1:p.Asn907Ser
XM_011532495.1:c.2252A>G	XP_011530797.1:p.Asn751Ser
XM_011532496.1:c.2195A>G	XP_011530798.1:p.Asn732Ser
NM_001320613.1:c.2795A>G	NP_001307542.1:p.Asn932Ser
NM_004036.4:c.2792A>G	NP_004027.2:p.Asn931Ser
XM_011532492.2:c.2918A>G	XP_011530794.1:p.Asn973Ser
XM_017003186.1:c.2858A>G	XP_016858675.1:p.Asn953Ser
XM_017003187.1:c.2849A>G	XP_016858676.1:p.Asn950Ser
XM_017003188.1:c.2915A>G	XP_016858677.1:p.Asn972Ser
XM_017003189.1:c.2777A>G	XP_016858678.1:p.Asn926Ser
XM_017003190.1:c.2654A>G	XP_016858679.1:p.Asn885Ser
XM_017003191.1:c.2282A>G	XP_016858680.1:p.Asn761Ser
XM_017003192.1:c.2072A>G	XP_016858681.1:p.Asn691Ser
XM_017003193.1:c.2069A>G	XP_016858682.1:p.Asn690Ser
NM_001320613.2:c.2795A>G	NP_001307542.1:p.Asn932Ser
NM_001377128.1:c.2858A>G	NP_001364057.1:p.Asn953Ser
NM_001377129.1:c.2654A>G	NP_001364058.1:p.Asn885Ser
NM_001377130.1:c.2332-670A>G	NP_001364059.1:n.2332-670A>G
NM_001377131.1:c.2069A>G	NP_001364060.1:p.Asn690Ser
NM_001377132.1:c.2792A>G	NP_001364061.1:p.Asn931Ser
NM_004036.5:c.2792A>G MANE Select	NP_004027.2:p.Asn931Ser