Canonical Allele Identifier: CA346063034

Gene: ADCY3

Linked Data

• ClinVar Variation Id: 3081589
• ClinVar RCV Id: RCV004370945
• dbSNP Id: rs1433512698
• gnomAD v2: 2-25046205-T-C
• gnomAD v3: 2-24823336-T-C
• gnomAD v4: 2-24823336-T-C
• MyVariant Identifiers: chr2:g.25046205T>C (hg19) ; chr2:g.24823336T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823336T>C , CM000664.2:g.24823336T>C	GRCh38
NC_000002.11:g.25046205T>C , CM000664.1:g.25046205T>C	GRCh37
NC_000002.10:g.24899709T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2759A>G	ENSP00000384484.2:p.Tyr920Cys
ENST00000679454.1:c.2756A>G MANE Select	ENSP00000505261.1:p.Tyr919Cys
ENST00000260600.9:c.2756A>G	ENSP00000260600.5:p.Tyr919Cys
ENST00000405392.5:c.2759A>G	ENSP00000384484.2:p.Tyr920Cys
ENST00000485887.1:n.28A>G
ENST00000606682.5:c.1697A>G	ENSP00000475652.1:p.Tyr566Cys
NM_004036.3:c.2756A>G	NP_004027.2:p.Tyr919Cys
XM_005264104.1:c.2759A>G	XP_005264161.1:p.Tyr920Cys
XM_005264105.1:c.2756A>G	XP_005264162.1:p.Tyr919Cys
XM_006711925.1:c.2825A>G	XP_006711988.1:p.Tyr942Cys
XM_011532489.1:c.2882A>G	XP_011530791.1:p.Tyr961Cys
XM_011532490.1:c.2879A>G	XP_011530792.1:p.Tyr960Cys
XM_011532491.1:c.2816A>G	XP_011530793.1:p.Tyr939Cys
XM_011532492.1:c.2882A>G	XP_011530794.1:p.Tyr961Cys
XM_011532493.1:c.2744A>G	XP_011530795.1:p.Tyr915Cys
XM_011532494.1:c.2684A>G	XP_011530796.1:p.Tyr895Cys
XM_011532495.1:c.2216A>G	XP_011530797.1:p.Tyr739Cys
XM_011532496.1:c.2159A>G	XP_011530798.1:p.Tyr720Cys
NM_001320613.1:c.2759A>G	NP_001307542.1:p.Tyr920Cys
NM_004036.4:c.2756A>G	NP_004027.2:p.Tyr919Cys
XM_011532492.2:c.2882A>G	XP_011530794.1:p.Tyr961Cys
XM_017003186.1:c.2822A>G	XP_016858675.1:p.Tyr941Cys
XM_017003187.1:c.2813A>G	XP_016858676.1:p.Tyr938Cys
XM_017003188.1:c.2879A>G	XP_016858677.1:p.Tyr960Cys
XM_017003189.1:c.2741A>G	XP_016858678.1:p.Tyr914Cys
XM_017003190.1:c.2618A>G	XP_016858679.1:p.Tyr873Cys
XM_017003191.1:c.2246A>G	XP_016858680.1:p.Tyr749Cys
XM_017003192.1:c.2036A>G	XP_016858681.1:p.Tyr679Cys
XM_017003193.1:c.2033A>G	XP_016858682.1:p.Tyr678Cys
NM_001320613.2:c.2759A>G	NP_001307542.1:p.Tyr920Cys
NM_001377128.1:c.2822A>G	NP_001364057.1:p.Tyr941Cys
NM_001377129.1:c.2618A>G	NP_001364058.1:p.Tyr873Cys
NM_001377130.1:c.2332-706A>G	NP_001364059.1:n.2332-706A>G
NM_001377131.1:c.2033A>G	NP_001364060.1:p.Tyr678Cys
NM_001377132.1:c.2756A>G	NP_001364061.1:p.Tyr919Cys
NM_004036.5:c.2756A>G MANE Select	NP_004027.2:p.Tyr919Cys