Canonical Allele Identifier: CA366241772

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522197A>C (hg19) ; chr6:g.157201063A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4679A>C	ENSP00000055163.8:p.Tyr1560Ser
ENST00000414678.8:c.4748A>C	ENSP00000412835.3:p.Tyr1583Ser
ENST00000637015.2:c.4967A>C	ENSP00000489729.2:p.Tyr1656Ser
ENST00000346085.10:c.4718A>C	ENSP00000344546.5:p.Tyr1573Ser
ENST00000350026.10:c.4430A>C	ENSP00000055163.7:p.Tyr1477Ser
ENST00000414678.7:c.2996A>C	ENSP00000412835.2:p.Tyr999Ser
ENST00000635849.1:c.2159A>C	ENSP00000490948.1:p.Tyr720Ser
ENST00000635957.1:c.1790A>C	ENSP00000490385.1:p.Tyr597Ser
ENST00000636227.1:n.3301A>C
ENST00000636254.1:n.758A>C
ENST00000636930.2:c.4838A>C MANE Select	ENSP00000490491.2:p.Tyr1613Ser
ENST00000636940.1:n.2835A>C
ENST00000637015.1:c.2206A>C
ENST00000637568.1:c.2120A>C
ENST00000637741.1:n.1504A>C
ENST00000637810.1:c.2180A>C	ENSP00000489636.1:p.Tyr727Ser
ENST00000637904.1:c.2339A>C	ENSP00000490550.1:p.Tyr780Ser
ENST00000647938.1:c.4469A>C	ENSP00000498155.1:p.Tyr1490Ser
ENST00000346085.9:c.4469A>C	ENSP00000344546.4:p.Tyr1490Ser
ENST00000350026.9:c.4430A>C	ENSP00000055163.7:p.Tyr1477Ser
ENST00000414678.6:c.2996A>C	ENSP00000412835.2:p.Tyr999Ser
NM_017519.2:c.4430A>C	NP_059989.2:p.Tyr1477Ser
NM_020732.3:c.4469A>C	NP_065783.3:p.Tyr1490Ser
XM_005267069.3:c.4589A>C	XP_005267126.2:p.Tyr1530Ser
XM_011535984.1:c.3668A>C	XP_011534286.1:p.Tyr1223Ser
XM_011535985.1:c.3488A>C	XP_011534287.1:p.Tyr1163Ser
XM_011535986.1:c.3248A>C	XP_011534288.1:p.Tyr1083Ser
XM_011535987.1:c.2867A>C	XP_011534289.1:p.Tyr956Ser
XM_011535988.1:c.1730A>C	XP_011534290.1:p.Tyr577Ser
NM_001346813.1:c.4589A>C	NP_001333742.1:p.Tyr1530Ser
NM_001363725.1:c.2339A>C	NP_001350654.1:p.Tyr780Ser
XM_011535984.2:c.4799A>C	XP_011534286.2:p.Tyr1600Ser
XM_011535988.3:c.1730A>C	XP_011534290.1:p.Tyr577Ser
XM_017011103.2:c.4700A>C	XP_016866592.1:p.Tyr1567Ser
XM_017011104.1:c.4670A>C	XP_016866593.1:p.Tyr1557Ser
XM_017011105.2:c.4640A>C	XP_016866594.1:p.Tyr1547Ser
XM_017011106.2:c.4511A>C	XP_016866595.1:p.Tyr1504Ser
XM_017011107.2:c.4490A>C	XP_016866596.1:p.Tyr1497Ser
XR_002956289.1:n.4785A>C
NM_001363725.2:c.2339A>C	NP_001350654.1:p.Tyr780Ser
NM_001371656.1:c.4718A>C	NP_001358585.1:p.Tyr1573Ser
NM_001374820.1:c.4718A>C	NP_001361749.1:p.Tyr1573Ser
NM_001374828.1:c.4838A>C MANE Select	NP_001361757.1:p.Tyr1613Ser
NM_017519.3:c.4679A>C	NP_059989.3:p.Tyr1560Ser