Canonical Allele Identifier: CA4067534

Gene: ARID1B

Linked Data

• dbSNP Id: rs779516798
• ExAC: 6:157511258 C / T
• gnomAD v2: 6-157511258-C-T
• gnomAD v4: 6-157190124-C-T
• COSMIC: COSM3622276 ; COSM3622277
• MyVariant Identifiers: chr6:g.157511258C>T (hg19) ; chr6:g.157190124C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190124C>T , CM000668.2:g.157190124C>T	GRCh38
NC_000006.11:g.157511258C>T , CM000668.1:g.157511258C>T	GRCh37
NC_000006.10:g.157552950C>T	NCBI36
NG_032093.1:g.417195C>T
NG_032093.2:g.417195C>T
NG_066624.1:g.419099C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3986C>T	ENSP00000055163.8:p.Pro1329Leu
ENST00000414678.8:c.4055C>T	ENSP00000412835.3:p.Pro1352Leu
ENST00000637015.2:c.4274C>T	ENSP00000489729.2:p.Pro1425Leu
ENST00000346085.10:c.4025C>T	ENSP00000344546.5:p.Pro1342Leu
ENST00000350026.10:c.3737C>T	ENSP00000055163.7:p.Pro1246Leu
ENST00000414678.7:c.2303C>T	ENSP00000412835.2:p.Pro768Leu
ENST00000635849.1:c.1466C>T	ENSP00000490948.1:p.Pro489Leu
ENST00000635957.1:c.1097C>T	ENSP00000490385.1:p.Pro366Leu
ENST00000636930.2:c.4145C>T MANE Select	ENSP00000490491.2:p.Pro1382Leu
ENST00000636940.1:n.2142C>T
ENST00000637015.1:c.1513C>T
ENST00000637568.1:c.1427C>T
ENST00000637741.1:n.811C>T
ENST00000637810.1:c.1487C>T	ENSP00000489636.1:p.Pro496Leu
ENST00000637904.1:c.1646C>T	ENSP00000490550.1:p.Pro549Leu
ENST00000647938.1:c.3776C>T	ENSP00000498155.1:p.Pro1259Leu
ENST00000346085.9:c.3776C>T	ENSP00000344546.4:p.Pro1259Leu
ENST00000350026.9:c.3737C>T	ENSP00000055163.7:p.Pro1246Leu
ENST00000414678.6:c.2303C>T	ENSP00000412835.2:p.Pro768Leu
NM_017519.2:c.3737C>T	NP_059989.2:p.Pro1246Leu
NM_020732.3:c.3776C>T	NP_065783.3:p.Pro1259Leu
XM_005267069.3:c.3896C>T	XP_005267126.2:p.Pro1299Leu
XM_011535984.1:c.2975C>T	XP_011534286.1:p.Pro992Leu
XM_011535985.1:c.2795C>T	XP_011534287.1:p.Pro932Leu
XM_011535986.1:c.2555C>T	XP_011534288.1:p.Pro852Leu
XM_011535987.1:c.2174C>T	XP_011534289.1:p.Pro725Leu
XM_011535988.1:c.1037C>T	XP_011534290.1:p.Pro346Leu
NM_001346813.1:c.3896C>T	NP_001333742.1:p.Pro1299Leu
NM_001363725.1:c.1646C>T	NP_001350654.1:p.Pro549Leu
XM_011535984.2:c.4106C>T	XP_011534286.2:p.Pro1369Leu
XM_011535988.3:c.1037C>T	XP_011534290.1:p.Pro346Leu
XM_017011103.2:c.4007C>T	XP_016866592.1:p.Pro1336Leu
XM_017011104.1:c.3977C>T	XP_016866593.1:p.Pro1326Leu
XM_017011105.2:c.3947C>T	XP_016866594.1:p.Pro1316Leu
XM_017011106.2:c.3818C>T	XP_016866595.1:p.Pro1273Leu
XM_017011107.2:c.3797C>T	XP_016866596.1:p.Pro1266Leu
XR_002956289.1:n.4189C>T
NM_001363725.2:c.1646C>T	NP_001350654.1:p.Pro549Leu
NM_001371656.1:c.4025C>T	NP_001358585.1:p.Pro1342Leu
NM_001374820.1:c.4025C>T	NP_001361749.1:p.Pro1342Leu
NM_001374828.1:c.4145C>T MANE Select	NP_001361757.1:p.Pro1382Leu
NM_017519.3:c.3986C>T	NP_059989.3:p.Pro1329Leu