Canonical Allele Identifier: CA425172188

Gene: ADCY3

Linked Data

• dbSNP Id: rs1668306466
• MyVariant Identifiers: chr2:g.25047337A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824468A>G , CM000664.2:g.24824468A>G	GRCh38
NC_000002.11:g.25047337A>G , CM000664.1:g.25047337A>G	GRCh37
NC_000002.10:g.24900841A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2649T>C	ENSP00000384484.2:p.Tyr883=
ENST00000679454.1:c.2646T>C MANE Select	ENSP00000505261.1:p.Tyr882=
ENST00000260600.9:c.2646T>C	ENSP00000260600.5:p.Tyr882=
ENST00000405392.5:c.2649T>C	ENSP00000384484.2:p.Tyr883=
ENST00000606682.5:c.1587T>C	ENSP00000475652.1:p.Tyr529=
NM_004036.3:c.2646T>C	NP_004027.2:p.Tyr882=
XM_005264104.1:c.2649T>C	XP_005264161.1:p.Tyr883=
XM_005264105.1:c.2646T>C	XP_005264162.1:p.Tyr882=
XM_006711925.1:c.2715T>C	XP_006711988.1:p.Tyr905=
XM_011532489.1:c.2772T>C	XP_011530791.1:p.Tyr924=
XM_011532490.1:c.2769T>C	XP_011530792.1:p.Tyr923=
XM_011532491.1:c.2706T>C	XP_011530793.1:p.Tyr902=
XM_011532492.1:c.2772T>C	XP_011530794.1:p.Tyr924=
XM_011532493.1:c.2634T>C	XP_011530795.1:p.Tyr878=
XM_011532494.1:c.2574T>C	XP_011530796.1:p.Tyr858=
XM_011532495.1:c.2106T>C	XP_011530797.1:p.Tyr702=
XM_011532496.1:c.2049T>C	XP_011530798.1:p.Tyr683=
NM_001320613.1:c.2649T>C	NP_001307542.1:p.Tyr883=
NM_004036.4:c.2646T>C	NP_004027.2:p.Tyr882=
XM_011532492.2:c.2772T>C	XP_011530794.1:p.Tyr924=
XM_017003186.1:c.2712T>C	XP_016858675.1:p.Tyr904=
XM_017003187.1:c.2703T>C	XP_016858676.1:p.Tyr901=
XM_017003188.1:c.2769T>C	XP_016858677.1:p.Tyr923=
XM_017003189.1:c.2631T>C	XP_016858678.1:p.Tyr877=
XM_017003190.1:c.2508T>C	XP_016858679.1:p.Tyr836=
XM_017003191.1:c.2136T>C	XP_016858680.1:p.Tyr712=
XM_017003192.1:c.1926T>C	XP_016858681.1:p.Tyr642=
XM_017003193.1:c.1923T>C	XP_016858682.1:p.Tyr641=
NM_001320613.2:c.2649T>C	NP_001307542.1:p.Tyr883=
NM_001377128.1:c.2712T>C	NP_001364057.1:p.Tyr904=
NM_001377129.1:c.2508T>C	NP_001364058.1:p.Tyr836=
NM_001377130.1:c.2241T>C	NP_001364059.1:p.Tyr747=
NM_001377131.1:c.1923T>C	NP_001364060.1:p.Tyr641=
NM_001377132.1:c.2646T>C	NP_001364061.1:p.Tyr882=
NM_004036.5:c.2646T>C MANE Select	NP_004027.2:p.Tyr882=