Canonical Allele Identifier: CA43679863

Gene: ADCY3

Linked Data

• dbSNP Id: rs538302749
• gnomAD v2: 2-25045780-A-G
• gnomAD v3: 2-24822911-A-G
• gnomAD v4: 2-24822911-A-G
• MyVariant Identifiers: chr2:g.25045780A>G (hg19) ; chr2:g.24822911A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24822911A>G , CM000664.2:g.24822911A>G	GRCh38
NC_000002.11:g.25045780A>G , CM000664.1:g.25045780A>G	GRCh37
NC_000002.10:g.24899284A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2887-281T>C	ENSP00000384484.2:n.2887-281T>C
ENST00000679454.1:c.2884-281T>C MANE Select	ENSP00000505261.1:n.2884-281T>C
ENST00000260600.9:c.2884-281T>C	ENSP00000260600.5:n.2884-281T>C
ENST00000405392.5:c.2887-281T>C	ENSP00000384484.2:n.2887-281T>C
ENST00000485887.1:n.156-281T>C
ENST00000606682.5:c.1825-281T>C	ENSP00000475652.1:n.1825-281T>C
NM_004036.3:c.2884-281T>C	NP_004027.2:n.2884-281T>C
XM_005264104.1:c.2887-281T>C	XP_005264161.1:n.2887-281T>C
XM_005264105.1:c.2884-281T>C	XP_005264162.1:n.2884-281T>C
XM_006711925.1:c.2953-281T>C	XP_006711988.1:n.2953-281T>C
XM_011532489.1:c.3010-281T>C	XP_011530791.1:n.3010-281T>C
XM_011532490.1:c.3007-281T>C	XP_011530792.1:n.3007-281T>C
XM_011532491.1:c.2944-281T>C	XP_011530793.1:n.2944-281T>C
XM_011532492.1:c.3010-281T>C	XP_011530794.1:n.3010-281T>C
XM_011532493.1:c.2872-281T>C	XP_011530795.1:n.2872-281T>C
XM_011532494.1:c.2812-281T>C	XP_011530796.1:n.2812-281T>C
XM_011532495.1:c.2344-281T>C	XP_011530797.1:n.2344-281T>C
XM_011532496.1:c.2287-281T>C	XP_011530798.1:n.2287-281T>C
NM_001320613.1:c.2887-281T>C	NP_001307542.1:n.2887-281T>C
NM_004036.4:c.2884-281T>C	NP_004027.2:n.2884-281T>C
XM_011532492.2:c.3010-281T>C	XP_011530794.1:n.3010-281T>C
XM_017003186.1:c.2950-281T>C	XP_016858675.1:n.2950-281T>C
XM_017003187.1:c.2941-281T>C	XP_016858676.1:n.2941-281T>C
XM_017003188.1:c.3007-281T>C	XP_016858677.1:n.3007-281T>C
XM_017003189.1:c.2869-281T>C	XP_016858678.1:n.2869-281T>C
XM_017003190.1:c.2746-281T>C	XP_016858679.1:n.2746-281T>C
XM_017003191.1:c.2374-281T>C	XP_016858680.1:n.2374-281T>C
XM_017003192.1:c.2164-281T>C	XP_016858681.1:n.2164-281T>C
XM_017003193.1:c.2161-281T>C	XP_016858682.1:n.2161-281T>C
NM_001320613.2:c.2887-281T>C	NP_001307542.1:n.2887-281T>C
NM_001377128.1:c.2950-281T>C	NP_001364057.1:n.2950-281T>C
NM_001377129.1:c.2746-281T>C	NP_001364058.1:n.2746-281T>C
NM_001377130.1:c.2332-281T>C	NP_001364059.1:n.2332-281T>C
NM_001377131.1:c.2161-281T>C	NP_001364060.1:n.2161-281T>C
NM_001377132.1:c.2884-281T>C	NP_001364061.1:n.2884-281T>C
NM_004036.5:c.2884-281T>C MANE Select	NP_004027.2:n.2884-281T>C