Canonical Allele Identifier: CA11691356
Gene: ART3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs6836703

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.76108994G>A , CM000666.2:g.76108994G>A GRCh38
NC_000004.11:g.77030147G>A , CM000666.1:g.77030147G>A GRCh37
NC_000004.10:g.77249171G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001130016.2:c.1036+1201G>A VV NP_001123488.1:p.=
NM_001130017.2:c.971-3392G>A VV NP_001123489.1:p.=
NM_001179.5:c.1003+1201G>A VV NP_001170.2:p.=
XM_005262997.1:c.1069+1201G>A XP_005263054.1:p.=
XM_005262999.1:c.1004-3392G>A XP_005263056.1:p.=
XM_005263003.1:c.941-3392G>A XP_005263060.1:p.=
XM_005263004.1:c.938-3392G>A XP_005263061.1:p.=
XM_006714218.1:c.1039+1201G>A XP_006714281.1:p.=
XM_006714220.1:c.973+1201G>A XP_006714283.1:p.=
XM_011531967.1:c.1037-942G>A XP_011530269.1:p.=
XM_011531968.1:c.1007-942G>A XP_011530270.1:p.=
XM_011531969.1:c.974-942G>A XP_011530271.1:p.=
XM_011531970.1:c.947-942G>A XP_011530272.1:p.=
XM_011531971.1:c.974-3392G>A XP_011530273.1:p.=
XM_017008210.2:c.914-3392G>A XP_016863699.1:p.=
XM_024454055.1:c.1069+1201G>A XP_024309823.1:p.=
XM_024454056.1:c.1006+1201G>A XP_024309824.1:p.=
XM_024454057.1:c.1004-3392G>A XP_024309825.1:p.=
XM_024454058.1:c.974-3392G>A XP_024309826.1:p.=
XM_024454059.1:c.973+1201G>A XP_024309827.1:p.=
XM_024454060.1:c.971-3392G>A XP_024309828.1:p.=
XM_024454061.1:c.941-3392G>A XP_024309829.1:p.=
XM_024454062.1:c.938-3392G>A XP_024309830.1:p.=
XM_024454063.1:c.938-3392G>A XP_024309831.1:p.=
XR_002959732.1:n.2393-3392G>A
XR_002959733.1:n.2834-3392G>A
ENST00000341029.9:c.971-3392G>A ENSP00000343843.5:p.=
ENST00000349321.7:c.1003+1201G>A ENSP00000304313.5:p.=
ENST00000355810.8:c.1036+1201G>A ENSP00000348064.4:p.=
ENST00000395688.7:n.172-3392G>A
ENST00000504112.5:n.268-3392G>A
ENST00000506313.1:n.259+1201G>A
ENST00000506667.5:n.235-3392G>A
ENST00000510669.5:n.389-2913G>A
ENST00000510863.1:n.578+1201G>A
ENST00000511188.1:n.325+1201G>A ENSP00000422249.1:p.=