Canonical Allele Identifier: CA346063759

Gene: ADCY3

Linked Data

• dbSNP Id: rs773980429
• gnomAD v4: 2-24824488-C-G
• MyVariant Identifiers: chr2:g.25047357C>G (hg19) ; chr2:g.24824488C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.24824488C>G , CM000664.2:g.24824488C>G	GRCh38
NC_000002.11:g.25047357C>G , CM000664.1:g.25047357C>G	GRCh37
NC_000002.10:g.24900861C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000405392.6:c.2629G>C	ENSP00000384484.2:p.Asp877His
ENST00000679454.1:c.2626G>C MANE Select	ENSP00000505261.1:p.Asp876His
ENST00000260600.9:c.2626G>C	ENSP00000260600.5:p.Asp876His
ENST00000405392.5:c.2629G>C	ENSP00000384484.2:p.Asp877His
ENST00000606682.5:c.1567G>C	ENSP00000475652.1:p.Asp523His
NM_004036.3:c.2626G>C	NP_004027.2:p.Asp876His
XM_005264104.1:c.2629G>C	XP_005264161.1:p.Asp877His
XM_005264105.1:c.2626G>C	XP_005264162.1:p.Asp876His
XM_006711925.1:c.2695G>C	XP_006711988.1:p.Asp899His
XM_011532489.1:c.2752G>C	XP_011530791.1:p.Asp918His
XM_011532490.1:c.2749G>C	XP_011530792.1:p.Asp917His
XM_011532491.1:c.2686G>C	XP_011530793.1:p.Asp896His
XM_011532492.1:c.2752G>C	XP_011530794.1:p.Asp918His
XM_011532493.1:c.2614G>C	XP_011530795.1:p.Asp872His
XM_011532494.1:c.2554G>C	XP_011530796.1:p.Asp852His
XM_011532495.1:c.2086G>C	XP_011530797.1:p.Asp696His
XM_011532496.1:c.2029G>C	XP_011530798.1:p.Asp677His
NM_001320613.1:c.2629G>C	NP_001307542.1:p.Asp877His
NM_004036.4:c.2626G>C	NP_004027.2:p.Asp876His
XM_011532492.2:c.2752G>C	XP_011530794.1:p.Asp918His
XM_017003186.1:c.2692G>C	XP_016858675.1:p.Asp898His
XM_017003187.1:c.2683G>C	XP_016858676.1:p.Asp895His
XM_017003188.1:c.2749G>C	XP_016858677.1:p.Asp917His
XM_017003189.1:c.2611G>C	XP_016858678.1:p.Asp871His
XM_017003190.1:c.2488G>C	XP_016858679.1:p.Asp830His
XM_017003191.1:c.2116G>C	XP_016858680.1:p.Asp706His
XM_017003192.1:c.1906G>C	XP_016858681.1:p.Asp636His
XM_017003193.1:c.1903G>C	XP_016858682.1:p.Asp635His
NM_001320613.2:c.2629G>C	NP_001307542.1:p.Asp877His
NM_001377128.1:c.2692G>C	NP_001364057.1:p.Asp898His
NM_001377129.1:c.2488G>C	NP_001364058.1:p.Asp830His
NM_001377130.1:c.2221G>C	NP_001364059.1:p.Asp741His
NM_001377131.1:c.1903G>C	NP_001364060.1:p.Asp635His
NM_001377132.1:c.2626G>C	NP_001364061.1:p.Asp876His
NM_004036.5:c.2626G>C MANE Select	NP_004027.2:p.Asp876His