Canonical Allele Identifier: CA425172187

Gene: ADCY3

Linked Data

• dbSNP Id: rs1157915112
• gnomAD v3: 2-24824461-G-T
• gnomAD v4: 2-24824461-G-T
• MyVariant Identifiers: chr2:g.25047330G>T (hg19) ; chr2:g.24824461G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824461G>T , CM000664.2:g.24824461G>T	GRCh38
NC_000002.11:g.25047330G>T , CM000664.1:g.25047330G>T	GRCh37
NC_000002.10:g.24900834G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000405392.6:c.2656C>A	ENSP00000384484.2:p.Arg886=
ENST00000679454.1:c.2653C>A MANE Select	ENSP00000505261.1:p.Arg885=
ENST00000260600.9:c.2653C>A	ENSP00000260600.5:p.Arg885=
ENST00000405392.5:c.2656C>A	ENSP00000384484.2:p.Arg886=
ENST00000606682.5:c.1594C>A	ENSP00000475652.1:p.Arg532=
NM_004036.3:c.2653C>A	NP_004027.2:p.Arg885=
XM_005264104.1:c.2656C>A	XP_005264161.1:p.Arg886=
XM_005264105.1:c.2653C>A	XP_005264162.1:p.Arg885=
XM_006711925.1:c.2722C>A	XP_006711988.1:p.Arg908=
XM_011532489.1:c.2779C>A	XP_011530791.1:p.Arg927=
XM_011532490.1:c.2776C>A	XP_011530792.1:p.Arg926=
XM_011532491.1:c.2713C>A	XP_011530793.1:p.Arg905=
XM_011532492.1:c.2779C>A	XP_011530794.1:p.Arg927=
XM_011532493.1:c.2641C>A	XP_011530795.1:p.Arg881=
XM_011532494.1:c.2581C>A	XP_011530796.1:p.Arg861=
XM_011532495.1:c.2113C>A	XP_011530797.1:p.Arg705=
XM_011532496.1:c.2056C>A	XP_011530798.1:p.Arg686=
NM_001320613.1:c.2656C>A	NP_001307542.1:p.Arg886=
NM_004036.4:c.2653C>A	NP_004027.2:p.Arg885=
XM_011532492.2:c.2779C>A	XP_011530794.1:p.Arg927=
XM_017003186.1:c.2719C>A	XP_016858675.1:p.Arg907=
XM_017003187.1:c.2710C>A	XP_016858676.1:p.Arg904=
XM_017003188.1:c.2776C>A	XP_016858677.1:p.Arg926=
XM_017003189.1:c.2638C>A	XP_016858678.1:p.Arg880=
XM_017003190.1:c.2515C>A	XP_016858679.1:p.Arg839=
XM_017003191.1:c.2143C>A	XP_016858680.1:p.Arg715=
XM_017003192.1:c.1933C>A	XP_016858681.1:p.Arg645=
XM_017003193.1:c.1930C>A	XP_016858682.1:p.Arg644=
NM_001320613.2:c.2656C>A	NP_001307542.1:p.Arg886=
NM_001377128.1:c.2719C>A	NP_001364057.1:p.Arg907=
NM_001377129.1:c.2515C>A	NP_001364058.1:p.Arg839=
NM_001377130.1:c.2248C>A	NP_001364059.1:p.Arg750=
NM_001377131.1:c.1930C>A	NP_001364060.1:p.Arg644=
NM_001377132.1:c.2653C>A	NP_001364061.1:p.Arg885=
NM_004036.5:c.2653C>A MANE Select	NP_004027.2:p.Arg885=