Canonical Allele Identifier: CA366241775

Gene: ARID1B

Linked Data

• dbSNP Id: rs758804576
• MyVariant Identifiers: chr6:g.157522197A>T (hg19) ; chr6:g.157201063A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201063A>T , CM000668.2:g.157201063A>T	GRCh38
NC_000006.11:g.157522197A>T , CM000668.1:g.157522197A>T	GRCh37
NC_000006.10:g.157563889A>T	NCBI36
NG_032093.1:g.428134A>T
NG_032093.2:g.428134A>T
NG_066624.1:g.430038A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4679A>T	ENSP00000055163.8:p.Tyr1560Phe
ENST00000414678.8:c.4748A>T	ENSP00000412835.3:p.Tyr1583Phe
ENST00000637015.2:c.4967A>T	ENSP00000489729.2:p.Tyr1656Phe
ENST00000346085.10:c.4718A>T	ENSP00000344546.5:p.Tyr1573Phe
ENST00000350026.10:c.4430A>T	ENSP00000055163.7:p.Tyr1477Phe
ENST00000414678.7:c.2996A>T	ENSP00000412835.2:p.Tyr999Phe
ENST00000635849.1:c.2159A>T	ENSP00000490948.1:p.Tyr720Phe
ENST00000635957.1:c.1790A>T	ENSP00000490385.1:p.Tyr597Phe
ENST00000636227.1:n.3301A>T
ENST00000636254.1:n.758A>T
ENST00000636930.2:c.4838A>T MANE Select	ENSP00000490491.2:p.Tyr1613Phe
ENST00000636940.1:n.2835A>T
ENST00000637015.1:c.2206A>T
ENST00000637568.1:c.2120A>T
ENST00000637741.1:n.1504A>T
ENST00000637810.1:c.2180A>T	ENSP00000489636.1:p.Tyr727Phe
ENST00000637904.1:c.2339A>T	ENSP00000490550.1:p.Tyr780Phe
ENST00000647938.1:c.4469A>T	ENSP00000498155.1:p.Tyr1490Phe
ENST00000346085.9:c.4469A>T	ENSP00000344546.4:p.Tyr1490Phe
ENST00000350026.9:c.4430A>T	ENSP00000055163.7:p.Tyr1477Phe
ENST00000414678.6:c.2996A>T	ENSP00000412835.2:p.Tyr999Phe
NM_017519.2:c.4430A>T	NP_059989.2:p.Tyr1477Phe
NM_020732.3:c.4469A>T	NP_065783.3:p.Tyr1490Phe
XM_005267069.3:c.4589A>T	XP_005267126.2:p.Tyr1530Phe
XM_011535984.1:c.3668A>T	XP_011534286.1:p.Tyr1223Phe
XM_011535985.1:c.3488A>T	XP_011534287.1:p.Tyr1163Phe
XM_011535986.1:c.3248A>T	XP_011534288.1:p.Tyr1083Phe
XM_011535987.1:c.2867A>T	XP_011534289.1:p.Tyr956Phe
XM_011535988.1:c.1730A>T	XP_011534290.1:p.Tyr577Phe
NM_001346813.1:c.4589A>T	NP_001333742.1:p.Tyr1530Phe
NM_001363725.1:c.2339A>T	NP_001350654.1:p.Tyr780Phe
XM_011535984.2:c.4799A>T	XP_011534286.2:p.Tyr1600Phe
XM_011535988.3:c.1730A>T	XP_011534290.1:p.Tyr577Phe
XM_017011103.2:c.4700A>T	XP_016866592.1:p.Tyr1567Phe
XM_017011104.1:c.4670A>T	XP_016866593.1:p.Tyr1557Phe
XM_017011105.2:c.4640A>T	XP_016866594.1:p.Tyr1547Phe
XM_017011106.2:c.4511A>T	XP_016866595.1:p.Tyr1504Phe
XM_017011107.2:c.4490A>T	XP_016866596.1:p.Tyr1497Phe
XR_002956289.1:n.4785A>T
NM_001363725.2:c.2339A>T	NP_001350654.1:p.Tyr780Phe
NM_001371656.1:c.4718A>T	NP_001358585.1:p.Tyr1573Phe
NM_001374820.1:c.4718A>T	NP_001361749.1:p.Tyr1573Phe
NM_001374828.1:c.4838A>T MANE Select	NP_001361757.1:p.Tyr1613Phe
NM_017519.3:c.4679A>T	NP_059989.3:p.Tyr1560Phe