Canonical Allele Identifier: CA425171945

Gene: ADCY3

Linked Data

• dbSNP Id: rs1476606402
• gnomAD v2: 2-25046102-A-G
• gnomAD v4: 2-24823233-A-G
• MyVariant Identifiers: chr2:g.25046102A>G (hg19) ; chr2:g.24823233A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823233A>G , CM000664.2:g.24823233A>G	GRCh38
NC_000002.11:g.25046102A>G , CM000664.1:g.25046102A>G	GRCh37
NC_000002.10:g.24899606A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2862T>C	ENSP00000384484.2:p.Asn954=
ENST00000679454.1:c.2859T>C MANE Select	ENSP00000505261.1:p.Asn953=
ENST00000260600.9:c.2859T>C	ENSP00000260600.5:p.Asn953=
ENST00000405392.5:c.2862T>C	ENSP00000384484.2:p.Asn954=
ENST00000485887.1:n.131T>C
ENST00000606682.5:c.1800T>C	ENSP00000475652.1:p.Asn600=
NM_004036.3:c.2859T>C	NP_004027.2:p.Asn953=
XM_005264104.1:c.2862T>C	XP_005264161.1:p.Asn954=
XM_005264105.1:c.2859T>C	XP_005264162.1:p.Asn953=
XM_006711925.1:c.2928T>C	XP_006711988.1:p.Asn976=
XM_011532489.1:c.2985T>C	XP_011530791.1:p.Asn995=
XM_011532490.1:c.2982T>C	XP_011530792.1:p.Asn994=
XM_011532491.1:c.2919T>C	XP_011530793.1:p.Asn973=
XM_011532492.1:c.2985T>C	XP_011530794.1:p.Asn995=
XM_011532493.1:c.2847T>C	XP_011530795.1:p.Asn949=
XM_011532494.1:c.2787T>C	XP_011530796.1:p.Asn929=
XM_011532495.1:c.2319T>C	XP_011530797.1:p.Asn773=
XM_011532496.1:c.2262T>C	XP_011530798.1:p.Asn754=
NM_001320613.1:c.2862T>C	NP_001307542.1:p.Asn954=
NM_004036.4:c.2859T>C	NP_004027.2:p.Asn953=
XM_011532492.2:c.2985T>C	XP_011530794.1:p.Asn995=
XM_017003186.1:c.2925T>C	XP_016858675.1:p.Asn975=
XM_017003187.1:c.2916T>C	XP_016858676.1:p.Asn972=
XM_017003188.1:c.2982T>C	XP_016858677.1:p.Asn994=
XM_017003189.1:c.2844T>C	XP_016858678.1:p.Asn948=
XM_017003190.1:c.2721T>C	XP_016858679.1:p.Asn907=
XM_017003191.1:c.2349T>C	XP_016858680.1:p.Asn783=
XM_017003192.1:c.2139T>C	XP_016858681.1:p.Asn713=
XM_017003193.1:c.2136T>C	XP_016858682.1:p.Asn712=
NM_001320613.2:c.2862T>C	NP_001307542.1:p.Asn954=
NM_001377128.1:c.2925T>C	NP_001364057.1:p.Asn975=
NM_001377129.1:c.2721T>C	NP_001364058.1:p.Asn907=
NM_001377130.1:c.2332-603T>C	NP_001364059.1:n.2332-603T>C
NM_001377131.1:c.2136T>C	NP_001364060.1:p.Asn712=
NM_001377132.1:c.2859T>C	NP_001364061.1:p.Asn953=
NM_004036.5:c.2859T>C MANE Select	NP_004027.2:p.Asn953=