Canonical Allele Identifier: CA1675522809

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201006T= , CM000668.2:g.157201006T=	GRCh38
NC_000006.11:g.157522140T= , CM000668.1:g.157522140T=	GRCh37
NC_000006.10:g.157563832T=	NCBI36
NG_032093.1:g.428077T=
NG_032093.2:g.428077T=
NG_066624.1:g.429981T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4622T=	ENSP00000055163.8:p.Met1541=
ENST00000414678.8:c.4691T=	ENSP00000412835.3:p.Met1564=
ENST00000637015.2:c.4910T=	ENSP00000489729.2:p.Met1637=
ENST00000346085.10:c.4661T=	ENSP00000344546.5:p.Met1554=
ENST00000350026.10:c.4373T=	ENSP00000055163.7:p.Met1458=
ENST00000414678.7:c.2939T=	ENSP00000412835.2:p.Met980=
ENST00000635849.1:c.2102T=	ENSP00000490948.1:p.Met701=
ENST00000635957.1:c.1733T=	ENSP00000490385.1:p.Met578=
ENST00000636227.1:n.3244T=
ENST00000636254.1:n.701T=
ENST00000636930.2:c.4781T= MANE Select	ENSP00000490491.2:p.Met1594=
ENST00000636940.1:n.2778T=
ENST00000637015.1:c.2149T=
ENST00000637568.1:c.2063T=
ENST00000637741.1:n.1447T=
ENST00000637810.1:c.2123T=	ENSP00000489636.1:p.Met708=
ENST00000637904.1:c.2282T=	ENSP00000490550.1:p.Met761=
ENST00000647938.1:c.4412T=	ENSP00000498155.1:p.Met1471=
ENST00000346085.9:c.4412T=	ENSP00000344546.4:p.Met1471=
ENST00000350026.9:c.4373T=	ENSP00000055163.7:p.Met1458=
ENST00000414678.6:c.2939T=	ENSP00000412835.2:p.Met980=
NM_017519.2:c.4373T=	NP_059989.2:p.Met1458=
NM_020732.3:c.4412T=	NP_065783.3:p.Met1471=
XM_005267069.3:c.4532T=	XP_005267126.2:p.Met1511=
XM_011535984.1:c.3611T=	XP_011534286.1:p.Met1204=
XM_011535985.1:c.3431T=	XP_011534287.1:p.Met1144=
XM_011535986.1:c.3191T=	XP_011534288.1:p.Met1064=
XM_011535987.1:c.2810T=	XP_011534289.1:p.Met937=
XM_011535988.1:c.1673T=	XP_011534290.1:p.Met558=
NM_001346813.1:c.4532T=	NP_001333742.1:p.Met1511=
NM_001363725.1:c.2282T=	NP_001350654.1:p.Met761=
XM_011535984.2:c.4742T=	XP_011534286.2:p.Met1581=
XM_011535988.3:c.1673T=	XP_011534290.1:p.Met558=
XM_017011103.2:c.4643T=	XP_016866592.1:p.Met1548=
XM_017011104.1:c.4613T=	XP_016866593.1:p.Met1538=
XM_017011105.2:c.4583T=	XP_016866594.1:p.Met1528=
XM_017011106.2:c.4454T=	XP_016866595.1:p.Met1485=
XM_017011107.2:c.4433T=	XP_016866596.1:p.Met1478=
XR_002956289.1:n.4728T=
NM_001363725.2:c.2282T=	NP_001350654.1:p.Met761=
NM_001371656.1:c.4661T=	NP_001358585.1:p.Met1554=
NM_001374820.1:c.4661T=	NP_001361749.1:p.Met1554=
NM_001374828.1:c.4781T= MANE Select	NP_001361757.1:p.Met1594=
NM_017519.3:c.4622T=	NP_059989.3:p.Met1541=