Canonical Allele Identifier: CA16042556
Gene: ARID1B HGNC NCBI

Linked Data

ClinVar Variation Id: 373273
ClinVar RCV Id: RCV000413077
dbSNP Id: rs1057518318

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.157148953T>C , CM000668.2:g.157148953T>C GRCh38
NC_000006.11:g.157470087T>C , CM000668.1:g.157470087T>C GRCh37
NC_000006.10:g.157511779T>C NCBI36
NG_032093.1:g.376024T>C
NG_032093.2:g.376024T>C
NG_066624.1:g.377928T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000319584.11:n.1103+2T>C ENSP00000313006.7:n.1103+2T>C
ENST00000346085.10:c.3128+2T>C ENSP00000344546.5:n.3128+2T>C
ENST00000350026.10:n.2840+2T>C ENSP00000055163.7:n.2840+2T>C
ENST00000414678.7:n.1247+2T>C ENSP00000412835.2:n.1247+2T>C
ENST00000452544.2:n.992T>C
ENST00000635849.1:c.410+2T>C ENSP00000490948.1:n.410+2T>C
ENST00000635957.1:n.44+2T>C ENSP00000490385.1:n.44+2T>C
ENST00000636426.1:n.225T>C
ENST00000636930.2:c.3089+2T>C MANE Select ENSP00000490491.2:n.3089+2T>C
ENST00000637015.1:n.328+2T>C
ENST00000637568.1:n.132+2T>C
ENST00000637810.1:c.590+2T>C ENSP00000489636.1:n.590+2T>C
ENST00000637904.1:c.590+2T>C ENSP00000490550.1:n.590+2T>C
ENST00000647938.1:n.2879+2T>C ENSP00000498155.1:n.2879+2T>C
ENST00000674190.1:n.1838+2T>C
ENST00000319584.10:n.1106+2T>C ENSP00000313006.6:n.1106+2T>C
ENST00000346085.9:c.2879+2T>C ENSP00000344546.4:n.2879+2T>C
ENST00000350026.9:c.2840+2T>C ENSP00000055163.7:n.2840+2T>C
ENST00000400790.3:n.41+2T>C ENSP00000383596.3:n.41+2T>C
ENST00000414678.6:n.1247+2T>C ENSP00000412835.2:n.1247+2T>C
ENST00000452544.1:n.938T>C
ENST00000478761.3:n.162+2T>C
NM_017519.2:n.2840+2T>C NP_059989.2:n.2840+2T>C
NM_020732.3:n.2879+2T>C NP_065783.3:n.2879+2T>C
XM_005267069.3:c.2840+2T>C XP_005267126.2:n.2840+2T>C
XM_011535984.1:c.1790+2T>C XP_011534286.1:n.1790+2T>C
XM_011535985.1:c.1610+2T>C XP_011534287.1:n.1610+2T>C
XM_011535986.1:c.1370+2T>C XP_011534288.1:n.1370+2T>C
XM_011535987.1:c.989+2T>C XP_011534289.1:n.989+2T>C
XM_011535988.1:c.-20+15746T>C XP_011534290.1:n.-20+15746T>C
NM_001346813.1:c.2840+2T>C NP_001333742.1:n.2840+2T>C
NM_001363725.1:c.590+2T>C NP_001350654.1:n.590+2T>C
XM_011535984.2:c.2921+2T>C XP_011534286.2:n.2921+2T>C
XM_011535988.3:c.-20+15746T>C XP_011534290.1:n.-20+15746T>C
XM_017011103.2:c.2923T>C XP_016866592.1:p.Tyr975His
XM_017011104.1:c.2921+2T>C XP_016866593.1:n.2921+2T>C
XM_017011105.2:c.2921+2T>C XP_016866594.1:n.2921+2T>C
XM_017011106.2:c.2921+2T>C XP_016866595.1:n.2921+2T>C
XM_017011107.2:c.2741+2T>C XP_016866596.1:n.2741+2T>C
XR_002956289.1:n.3004+2T>C
NM_001363725.2:c.590+2T>C NP_001350654.1:n.590+2T>C
NM_001371656.1:c.3128+2T>C NP_001358585.1:n.3128+2T>C
NM_001374820.1:c.3128+2T>C NP_001361749.1:n.3128+2T>C
NM_001374828.1:c.3089+2T>C MANE Select NP_001361757.1:n.3089+2T>C
NM_017519.3:c.3089+2T>C NP_059989.3:n.3089+2T>C