Canonical Allele Identifier: CA4067536

Gene: ARID1B

Linked Data

• dbSNP Id: rs763978832
• ExAC: 6:157511260 TACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG / T
• gnomAD v2: 6-157511260-TACCAGCAGGGCATGAGCATGCCCGATGTGATGGGCAGG-T
• MyVariant Identifiers: chr6:g.157511261_157511298del (hg19) ; chr6:g.157190127_157190164del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190128_157190165del , CM000668.2:g.157190128_157190165del	GRCh38
NC_000006.11:g.157511262_157511299del , CM000668.1:g.157511262_157511299del	GRCh37
NC_000006.10:g.157552954_157552991del	NCBI36
NG_032093.1:g.417199_417236del
NG_032093.2:g.417199_417236del
NG_066624.1:g.419103_419140del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3990_4027del	ENSP00000055163.8:p.Gln1331AlafsTer3
ENST00000414678.8:c.4059_4096del	ENSP00000412835.3:p.Gln1354AlafsTer3
ENST00000637015.2:c.4278_4315del	ENSP00000489729.2:p.Gln1427AlafsTer3
ENST00000346085.10:c.4029_4066del	ENSP00000344546.5:p.Gln1344AlafsTer3
ENST00000350026.10:c.3741_3778del	ENSP00000055163.7:p.Gln1248AlafsTer3
ENST00000414678.7:c.2307_2344del	ENSP00000412835.2:p.Gln770AlafsTer3
ENST00000635849.1:c.1470_1507del	ENSP00000490948.1:p.Gln491AlafsTer3
ENST00000635957.1:c.1101_1138del	ENSP00000490385.1:p.Gln368AlafsTer3
ENST00000636930.2:c.4149_4186del MANE Select	ENSP00000490491.2:p.Gln1384AlafsTer3
ENST00000636940.1:n.2146_2183del
ENST00000637015.1:c.1517_1554del
ENST00000637568.1:c.1431_1468del
ENST00000637741.1:n.815_852del
ENST00000637810.1:c.1491_1528del	ENSP00000489636.1:p.Gln498AlafsTer3
ENST00000637904.1:c.1650_1687del	ENSP00000490550.1:p.Gln551AlafsTer3
ENST00000647938.1:c.3780_3817del	ENSP00000498155.1:p.Gln1261AlafsTer3
ENST00000346085.9:c.3780_3817del	ENSP00000344546.4:p.Gln1261AlafsTer3
ENST00000350026.9:c.3741_3778del	ENSP00000055163.7:p.Gln1248AlafsTer3
ENST00000414678.6:c.2307_2344del	ENSP00000412835.2:p.Gln770AlafsTer3
NM_017519.2:c.3741_3778del	NP_059989.2:p.Gln1248AlafsTer3
NM_020732.3:c.3780_3817del	NP_065783.3:p.Gln1261AlafsTer3
XM_005267069.3:c.3900_3937del	XP_005267126.2:p.Gln1301AlafsTer3
XM_011535984.1:c.2979_3016del	XP_011534286.1:p.Gln994AlafsTer3
XM_011535985.1:c.2799_2836del	XP_011534287.1:p.Gln934AlafsTer3
XM_011535986.1:c.2559_2596del	XP_011534288.1:p.Gln854AlafsTer3
XM_011535987.1:c.2178_2215del	XP_011534289.1:p.Gln727AlafsTer3
XM_011535988.1:c.1041_1078del	XP_011534290.1:p.Gln348AlafsTer3
NM_001346813.1:c.3900_3937del	NP_001333742.1:p.Gln1301AlafsTer3
NM_001363725.1:c.1650_1687del	NP_001350654.1:p.Gln551AlafsTer3
XM_011535984.2:c.4110_4147del	XP_011534286.2:p.Gln1371AlafsTer3
XM_011535988.3:c.1041_1078del	XP_011534290.1:p.Gln348AlafsTer3
XM_017011103.2:c.4011_4048del	XP_016866592.1:p.Gln1338AlafsTer3
XM_017011104.1:c.3981_4018del	XP_016866593.1:p.Gln1328AlafsTer3
XM_017011105.2:c.3951_3988del	XP_016866594.1:p.Gln1318AlafsTer3
XM_017011106.2:c.3822_3859del	XP_016866595.1:p.Gln1275AlafsTer3
XM_017011107.2:c.3801_3838del	XP_016866596.1:p.Gln1268AlafsTer3
XR_002956289.1:n.4193_4230del
NM_001363725.2:c.1650_1687del	NP_001350654.1:p.Gln551AlafsTer3
NM_001371656.1:c.4029_4066del	NP_001358585.1:p.Gln1344AlafsTer3
NM_001374820.1:c.4029_4066del	NP_001361749.1:p.Gln1344AlafsTer3
NM_001374828.1:c.4149_4186del MANE Select	NP_001361757.1:p.Gln1384AlafsTer3
NM_017519.3:c.3990_4027del	NP_059989.3:p.Gln1331AlafsTer3