Canonical Allele Identifier: CA1675523451

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201345T= , CM000668.2:g.157201345T=	GRCh38
NC_000006.11:g.157522479T= , CM000668.1:g.157522479T=	GRCh37
NC_000006.10:g.157564171T=	NCBI36
NG_032093.1:g.428416T=
NG_032093.2:g.428416T=
NG_066624.1:g.430320T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4961T=	ENSP00000055163.8:p.Met1654=
ENST00000414678.8:c.5030T=	ENSP00000412835.3:p.Met1677=
ENST00000637015.2:c.5249T=	ENSP00000489729.2:p.Met1750=
ENST00000346085.10:c.5000T=	ENSP00000344546.5:p.Met1667=
ENST00000350026.10:c.4712T=	ENSP00000055163.7:p.Met1571=
ENST00000414678.7:c.3278T=	ENSP00000412835.2:p.Met1093=
ENST00000635849.1:c.2441T=	ENSP00000490948.1:p.Met814=
ENST00000635957.1:c.2072T=	ENSP00000490385.1:p.Met691=
ENST00000636227.1:n.3583T=
ENST00000636254.1:n.1040T=
ENST00000636930.2:c.5120T= MANE Select	ENSP00000490491.2:p.Met1707=
ENST00000636940.1:n.3117T=
ENST00000637015.1:c.2488T=
ENST00000637568.1:c.2402T=
ENST00000637741.1:n.1786T=
ENST00000637810.1:c.2462T=	ENSP00000489636.1:p.Met821=
ENST00000637904.1:c.2621T=	ENSP00000490550.1:p.Met874=
ENST00000647938.1:c.4751T=	ENSP00000498155.1:p.Met1584=
ENST00000346085.9:c.4751T=	ENSP00000344546.4:p.Met1584=
ENST00000350026.9:c.4712T=	ENSP00000055163.7:p.Met1571=
ENST00000414678.6:c.3278T=	ENSP00000412835.2:p.Met1093=
NM_017519.2:c.4712T=	NP_059989.2:p.Met1571=
NM_020732.3:c.4751T=	NP_065783.3:p.Met1584=
XM_005267069.3:c.4871T=	XP_005267126.2:p.Met1624=
XM_011535984.1:c.3950T=	XP_011534286.1:p.Met1317=
XM_011535985.1:c.3770T=	XP_011534287.1:p.Met1257=
XM_011535986.1:c.3530T=	XP_011534288.1:p.Met1177=
XM_011535987.1:c.3149T=	XP_011534289.1:p.Met1050=
XM_011535988.1:c.2012T=	XP_011534290.1:p.Met671=
NM_001346813.1:c.4871T=	NP_001333742.1:p.Met1624=
NM_001363725.1:c.2621T=	NP_001350654.1:p.Met874=
XM_011535984.2:c.5081T=	XP_011534286.2:p.Met1694=
XM_011535988.3:c.2012T=	XP_011534290.1:p.Met671=
XM_017011103.2:c.4982T=	XP_016866592.1:p.Met1661=
XM_017011104.1:c.4952T=	XP_016866593.1:p.Met1651=
XM_017011105.2:c.4922T=	XP_016866594.1:p.Met1641=
XM_017011106.2:c.4793T=	XP_016866595.1:p.Met1598=
XM_017011107.2:c.4772T=	XP_016866596.1:p.Met1591=
XR_002956289.1:n.5067T=
NM_001363725.2:c.2621T=	NP_001350654.1:p.Met874=
NM_001371656.1:c.5000T=	NP_001358585.1:p.Met1667=
NM_001374820.1:c.5000T=	NP_001361749.1:p.Met1667=
NM_001374828.1:c.5120T= MANE Select	NP_001361757.1:p.Met1707=
NM_017519.3:c.4961T=	NP_059989.3:p.Met1654=