Canonical Allele Identifier: CA346063650

Gene: ADCY3

Linked Data

• dbSNP Id: rs1402941862
• gnomAD v2: 2-25047326-C-T
• gnomAD v4: 2-24824457-C-T
• MyVariant Identifiers: chr2:g.25047326C>T (hg19) ; chr2:g.24824457C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824457C>T , CM000664.2:g.24824457C>T	GRCh38
NC_000002.11:g.25047326C>T , CM000664.1:g.25047326C>T	GRCh37
NC_000002.10:g.24900830C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2660G>A	ENSP00000384484.2:p.Arg887His
ENST00000679454.1:c.2657G>A MANE Select	ENSP00000505261.1:p.Arg886His
ENST00000260600.9:c.2657G>A	ENSP00000260600.5:p.Arg886His
ENST00000405392.5:c.2660G>A	ENSP00000384484.2:p.Arg887His
ENST00000606682.5:c.1598G>A	ENSP00000475652.1:p.Arg533His
NM_004036.3:c.2657G>A	NP_004027.2:p.Arg886His
XM_005264104.1:c.2660G>A	XP_005264161.1:p.Arg887His
XM_005264105.1:c.2657G>A	XP_005264162.1:p.Arg886His
XM_006711925.1:c.2726G>A	XP_006711988.1:p.Arg909His
XM_011532489.1:c.2783G>A	XP_011530791.1:p.Arg928His
XM_011532490.1:c.2780G>A	XP_011530792.1:p.Arg927His
XM_011532491.1:c.2717G>A	XP_011530793.1:p.Arg906His
XM_011532492.1:c.2783G>A	XP_011530794.1:p.Arg928His
XM_011532493.1:c.2645G>A	XP_011530795.1:p.Arg882His
XM_011532494.1:c.2585G>A	XP_011530796.1:p.Arg862His
XM_011532495.1:c.2117G>A	XP_011530797.1:p.Arg706His
XM_011532496.1:c.2060G>A	XP_011530798.1:p.Arg687His
NM_001320613.1:c.2660G>A	NP_001307542.1:p.Arg887His
NM_004036.4:c.2657G>A	NP_004027.2:p.Arg886His
XM_011532492.2:c.2783G>A	XP_011530794.1:p.Arg928His
XM_017003186.1:c.2723G>A	XP_016858675.1:p.Arg908His
XM_017003187.1:c.2714G>A	XP_016858676.1:p.Arg905His
XM_017003188.1:c.2780G>A	XP_016858677.1:p.Arg927His
XM_017003189.1:c.2642G>A	XP_016858678.1:p.Arg881His
XM_017003190.1:c.2519G>A	XP_016858679.1:p.Arg840His
XM_017003191.1:c.2147G>A	XP_016858680.1:p.Arg716His
XM_017003192.1:c.1937G>A	XP_016858681.1:p.Arg646His
XM_017003193.1:c.1934G>A	XP_016858682.1:p.Arg645His
NM_001320613.2:c.2660G>A	NP_001307542.1:p.Arg887His
NM_001377128.1:c.2723G>A	NP_001364057.1:p.Arg908His
NM_001377129.1:c.2519G>A	NP_001364058.1:p.Arg840His
NM_001377130.1:c.2252G>A	NP_001364059.1:p.Arg751His
NM_001377131.1:c.1934G>A	NP_001364060.1:p.Arg645His
NM_001377132.1:c.2657G>A	NP_001364061.1:p.Arg886His
NM_004036.5:c.2657G>A MANE Select	NP_004027.2:p.Arg886His