Canonical Allele Identifier: CA346062506

Gene: ADCY3

Linked Data

• dbSNP Id: rs1193146288
• gnomAD v2: 2-25046095-T-C
• MyVariant Identifiers: chr2:g.25046095T>C (hg19) ; chr2:g.24823226T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24823226T>C , CM000664.2:g.24823226T>C	GRCh38
NC_000002.11:g.25046095T>C , CM000664.1:g.25046095T>C	GRCh37
NC_000002.10:g.24899599T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2869A>G	ENSP00000384484.2:p.Ile957Val
ENST00000679454.1:c.2866A>G MANE Select	ENSP00000505261.1:p.Ile956Val
ENST00000260600.9:c.2866A>G	ENSP00000260600.5:p.Ile956Val
ENST00000405392.5:c.2869A>G	ENSP00000384484.2:p.Ile957Val
ENST00000485887.1:n.138A>G
ENST00000606682.5:c.1807A>G	ENSP00000475652.1:p.Ile603Val
NM_004036.3:c.2866A>G	NP_004027.2:p.Ile956Val
XM_005264104.1:c.2869A>G	XP_005264161.1:p.Ile957Val
XM_005264105.1:c.2866A>G	XP_005264162.1:p.Ile956Val
XM_006711925.1:c.2935A>G	XP_006711988.1:p.Ile979Val
XM_011532489.1:c.2992A>G	XP_011530791.1:p.Ile998Val
XM_011532490.1:c.2989A>G	XP_011530792.1:p.Ile997Val
XM_011532491.1:c.2926A>G	XP_011530793.1:p.Ile976Val
XM_011532492.1:c.2992A>G	XP_011530794.1:p.Ile998Val
XM_011532493.1:c.2854A>G	XP_011530795.1:p.Ile952Val
XM_011532494.1:c.2794A>G	XP_011530796.1:p.Ile932Val
XM_011532495.1:c.2326A>G	XP_011530797.1:p.Ile776Val
XM_011532496.1:c.2269A>G	XP_011530798.1:p.Ile757Val
NM_001320613.1:c.2869A>G	NP_001307542.1:p.Ile957Val
NM_004036.4:c.2866A>G	NP_004027.2:p.Ile956Val
XM_011532492.2:c.2992A>G	XP_011530794.1:p.Ile998Val
XM_017003186.1:c.2932A>G	XP_016858675.1:p.Ile978Val
XM_017003187.1:c.2923A>G	XP_016858676.1:p.Ile975Val
XM_017003188.1:c.2989A>G	XP_016858677.1:p.Ile997Val
XM_017003189.1:c.2851A>G	XP_016858678.1:p.Ile951Val
XM_017003190.1:c.2728A>G	XP_016858679.1:p.Ile910Val
XM_017003191.1:c.2356A>G	XP_016858680.1:p.Ile786Val
XM_017003192.1:c.2146A>G	XP_016858681.1:p.Ile716Val
XM_017003193.1:c.2143A>G	XP_016858682.1:p.Ile715Val
NM_001320613.2:c.2869A>G	NP_001307542.1:p.Ile957Val
NM_001377128.1:c.2932A>G	NP_001364057.1:p.Ile978Val
NM_001377129.1:c.2728A>G	NP_001364058.1:p.Ile910Val
NM_001377130.1:c.2332-596A>G	NP_001364059.1:n.2332-596A>G
NM_001377131.1:c.2143A>G	NP_001364060.1:p.Ile715Val
NM_001377132.1:c.2866A>G	NP_001364061.1:p.Ile956Val
NM_004036.5:c.2866A>G MANE Select	NP_004027.2:p.Ile956Val