Canonical Allele Identifier: CA4067708

Gene: ARID1B

Linked Data

• dbSNP Id: rs775015868
• ExAC: 6:157522136 G / T
• gnomAD v2: 6-157522136-G-T
• MyVariant Identifiers: chr6:g.157522136G>T (hg19) ; chr6:g.157201002G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201002G>T , CM000668.2:g.157201002G>T	GRCh38
NC_000006.11:g.157522136G>T , CM000668.1:g.157522136G>T	GRCh37
NC_000006.10:g.157563828G>T	NCBI36
NG_032093.1:g.428073G>T
NG_032093.2:g.428073G>T
NG_066624.1:g.429977G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4618G>T	ENSP00000055163.8:p.Asp1540Tyr
ENST00000414678.8:c.4687G>T	ENSP00000412835.3:p.Asp1563Tyr
ENST00000637015.2:c.4906G>T	ENSP00000489729.2:p.Asp1636Tyr
ENST00000346085.10:c.4657G>T	ENSP00000344546.5:p.Asp1553Tyr
ENST00000350026.10:c.4369G>T	ENSP00000055163.7:p.Asp1457Tyr
ENST00000414678.7:c.2935G>T	ENSP00000412835.2:p.Asp979Tyr
ENST00000635849.1:c.2098G>T	ENSP00000490948.1:p.Asp700Tyr
ENST00000635957.1:c.1729G>T	ENSP00000490385.1:p.Asp577Tyr
ENST00000636227.1:n.3240G>T
ENST00000636254.1:n.697G>T
ENST00000636930.2:c.4777G>T MANE Select	ENSP00000490491.2:p.Asp1593Tyr
ENST00000636940.1:n.2774G>T
ENST00000637015.1:c.2145G>T
ENST00000637568.1:c.2059G>T
ENST00000637741.1:n.1443G>T
ENST00000637810.1:c.2119G>T	ENSP00000489636.1:p.Asp707Tyr
ENST00000637904.1:c.2278G>T	ENSP00000490550.1:p.Asp760Tyr
ENST00000647938.1:c.4408G>T	ENSP00000498155.1:p.Asp1470Tyr
ENST00000346085.9:c.4408G>T	ENSP00000344546.4:p.Asp1470Tyr
ENST00000350026.9:c.4369G>T	ENSP00000055163.7:p.Asp1457Tyr
ENST00000414678.6:c.2935G>T	ENSP00000412835.2:p.Asp979Tyr
NM_017519.2:c.4369G>T	NP_059989.2:p.Asp1457Tyr
NM_020732.3:c.4408G>T	NP_065783.3:p.Asp1470Tyr
XM_005267069.3:c.4528G>T	XP_005267126.2:p.Asp1510Tyr
XM_011535984.1:c.3607G>T	XP_011534286.1:p.Asp1203Tyr
XM_011535985.1:c.3427G>T	XP_011534287.1:p.Asp1143Tyr
XM_011535986.1:c.3187G>T	XP_011534288.1:p.Asp1063Tyr
XM_011535987.1:c.2806G>T	XP_011534289.1:p.Asp936Tyr
XM_011535988.1:c.1669G>T	XP_011534290.1:p.Asp557Tyr
NM_001346813.1:c.4528G>T	NP_001333742.1:p.Asp1510Tyr
NM_001363725.1:c.2278G>T	NP_001350654.1:p.Asp760Tyr
XM_011535984.2:c.4738G>T	XP_011534286.2:p.Asp1580Tyr
XM_011535988.3:c.1669G>T	XP_011534290.1:p.Asp557Tyr
XM_017011103.2:c.4639G>T	XP_016866592.1:p.Asp1547Tyr
XM_017011104.1:c.4609G>T	XP_016866593.1:p.Asp1537Tyr
XM_017011105.2:c.4579G>T	XP_016866594.1:p.Asp1527Tyr
XM_017011106.2:c.4450G>T	XP_016866595.1:p.Asp1484Tyr
XM_017011107.2:c.4429G>T	XP_016866596.1:p.Asp1477Tyr
XR_002956289.1:n.4724G>T
NM_001363725.2:c.2278G>T	NP_001350654.1:p.Asp760Tyr
NM_001371656.1:c.4657G>T	NP_001358585.1:p.Asp1553Tyr
NM_001374820.1:c.4657G>T	NP_001361749.1:p.Asp1553Tyr
NM_001374828.1:c.4777G>T MANE Select	NP_001361757.1:p.Asp1593Tyr
NM_017519.3:c.4618G>T	NP_059989.3:p.Asp1540Tyr