Canonical Allele Identifier: CA366241495

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522146A>T (hg19) ; chr6:g.157201012A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201012A>T , CM000668.2:g.157201012A>T	GRCh38
NC_000006.11:g.157522146A>T , CM000668.1:g.157522146A>T	GRCh37
NC_000006.10:g.157563838A>T	NCBI36
NG_032093.1:g.428083A>T
NG_032093.2:g.428083A>T
NG_066624.1:g.429987A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4628A>T	ENSP00000055163.8:p.Tyr1543Phe
ENST00000414678.8:c.4697A>T	ENSP00000412835.3:p.Tyr1566Phe
ENST00000637015.2:c.4916A>T	ENSP00000489729.2:p.Tyr1639Phe
ENST00000346085.10:c.4667A>T	ENSP00000344546.5:p.Tyr1556Phe
ENST00000350026.10:c.4379A>T	ENSP00000055163.7:p.Tyr1460Phe
ENST00000414678.7:c.2945A>T	ENSP00000412835.2:p.Tyr982Phe
ENST00000635849.1:c.2108A>T	ENSP00000490948.1:p.Tyr703Phe
ENST00000635957.1:c.1739A>T	ENSP00000490385.1:p.Tyr580Phe
ENST00000636227.1:n.3250A>T
ENST00000636254.1:n.707A>T
ENST00000636930.2:c.4787A>T MANE Select	ENSP00000490491.2:p.Tyr1596Phe
ENST00000636940.1:n.2784A>T
ENST00000637015.1:c.2155A>T
ENST00000637568.1:c.2069A>T
ENST00000637741.1:n.1453A>T
ENST00000637810.1:c.2129A>T	ENSP00000489636.1:p.Tyr710Phe
ENST00000637904.1:c.2288A>T	ENSP00000490550.1:p.Tyr763Phe
ENST00000647938.1:c.4418A>T	ENSP00000498155.1:p.Tyr1473Phe
ENST00000346085.9:c.4418A>T	ENSP00000344546.4:p.Tyr1473Phe
ENST00000350026.9:c.4379A>T	ENSP00000055163.7:p.Tyr1460Phe
ENST00000414678.6:c.2945A>T	ENSP00000412835.2:p.Tyr982Phe
NM_017519.2:c.4379A>T	NP_059989.2:p.Tyr1460Phe
NM_020732.3:c.4418A>T	NP_065783.3:p.Tyr1473Phe
XM_005267069.3:c.4538A>T	XP_005267126.2:p.Tyr1513Phe
XM_011535984.1:c.3617A>T	XP_011534286.1:p.Tyr1206Phe
XM_011535985.1:c.3437A>T	XP_011534287.1:p.Tyr1146Phe
XM_011535986.1:c.3197A>T	XP_011534288.1:p.Tyr1066Phe
XM_011535987.1:c.2816A>T	XP_011534289.1:p.Tyr939Phe
XM_011535988.1:c.1679A>T	XP_011534290.1:p.Tyr560Phe
NM_001346813.1:c.4538A>T	NP_001333742.1:p.Tyr1513Phe
NM_001363725.1:c.2288A>T	NP_001350654.1:p.Tyr763Phe
XM_011535984.2:c.4748A>T	XP_011534286.2:p.Tyr1583Phe
XM_011535988.3:c.1679A>T	XP_011534290.1:p.Tyr560Phe
XM_017011103.2:c.4649A>T	XP_016866592.1:p.Tyr1550Phe
XM_017011104.1:c.4619A>T	XP_016866593.1:p.Tyr1540Phe
XM_017011105.2:c.4589A>T	XP_016866594.1:p.Tyr1530Phe
XM_017011106.2:c.4460A>T	XP_016866595.1:p.Tyr1487Phe
XM_017011107.2:c.4439A>T	XP_016866596.1:p.Tyr1480Phe
XR_002956289.1:n.4734A>T
NM_001363725.2:c.2288A>T	NP_001350654.1:p.Tyr763Phe
NM_001371656.1:c.4667A>T	NP_001358585.1:p.Tyr1556Phe
NM_001374820.1:c.4667A>T	NP_001361749.1:p.Tyr1556Phe
NM_001374828.1:c.4787A>T MANE Select	NP_001361757.1:p.Tyr1596Phe
NM_017519.3:c.4628A>T	NP_059989.3:p.Tyr1543Phe