Canonical Allele Identifier: CA1675517078

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148924A= , CM000668.2:g.157148924A=	GRCh38
NC_000006.11:g.157470058A= , CM000668.1:g.157470058A=	GRCh37
NC_000006.10:g.157511750A=	NCBI36
NG_032093.1:g.375995A=
NG_032093.2:g.375995A=
NG_066624.1:g.377899A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3062A=	ENSP00000055163.8:p.Gln1021=
ENST00000414678.8:c.2972A=	ENSP00000412835.3:p.Gln991=
ENST00000637015.2:c.3062A=	ENSP00000489729.2:p.Gln1021=
ENST00000319584.11:c.1076A=	ENSP00000313006.7:p.Gln359=
ENST00000346085.10:c.3101A=	ENSP00000344546.5:p.Gln1034=
ENST00000350026.10:c.2813A=	ENSP00000055163.7:p.Gln938=
ENST00000414678.7:c.1220A=	ENSP00000412835.2:p.Gln407=
ENST00000452544.2:n.963A=
ENST00000635849.1:c.383A=	ENSP00000490948.1:p.Gln128=
ENST00000635957.1:c.17A=	ENSP00000490385.1:p.Gln6=
ENST00000636426.1:n.196A=
ENST00000636930.2:c.3062A= MANE Select	ENSP00000490491.2:p.Gln1021=
ENST00000637015.1:c.301A=
ENST00000637568.1:c.105A=
ENST00000637810.1:c.563A=	ENSP00000489636.1:p.Gln188=
ENST00000637904.1:c.563A=	ENSP00000490550.1:p.Gln188=
ENST00000647938.1:c.2852A=	ENSP00000498155.1:p.Gln951=
ENST00000674190.1:n.1811A=
ENST00000319584.10:c.1079A=	ENSP00000313006.6:p.Gln360=
ENST00000346085.9:c.2852A=	ENSP00000344546.4:p.Gln951=
ENST00000350026.9:c.2813A=	ENSP00000055163.7:p.Gln938=
ENST00000400790.3:c.14A=	ENSP00000383596.3:p.Gln5=
ENST00000414678.6:c.1220A=	ENSP00000412835.2:p.Gln407=
ENST00000452544.1:n.909A=
ENST00000478761.3:c.135A=
NM_017519.2:c.2813A=	NP_059989.2:p.Gln938=
NM_020732.3:c.2852A=	NP_065783.3:p.Gln951=
XM_005267069.3:c.2813A=	XP_005267126.2:p.Gln938=
XM_011535984.1:c.1763A=	XP_011534286.1:p.Gln588=
XM_011535985.1:c.1583A=	XP_011534287.1:p.Gln528=
XM_011535986.1:c.1343A=	XP_011534288.1:p.Gln448=
XM_011535987.1:c.962A=	XP_011534289.1:p.Gln321=
XM_011535988.1:c.-20+15717A=	XP_011534290.1:n.-20+15717A=
NM_001346813.1:c.2813A=	NP_001333742.1:p.Gln938=
NM_001363725.1:c.563A=	NP_001350654.1:p.Gln188=
XM_011535984.2:c.2894A=	XP_011534286.2:p.Gln965=
XM_011535988.3:c.-20+15717A=	XP_011534290.1:n.-20+15717A=
XM_017011103.2:c.2894A=	XP_016866592.1:p.Gln965=
XM_017011104.1:c.2894A=	XP_016866593.1:p.Gln965=
XM_017011105.2:c.2894A=	XP_016866594.1:p.Gln965=
XM_017011106.2:c.2894A=	XP_016866595.1:p.Gln965=
XM_017011107.2:c.2714A=	XP_016866596.1:p.Gln905=
XR_002956289.1:n.2977A=
NM_001363725.2:c.563A=	NP_001350654.1:p.Gln188=
NM_001371656.1:c.3101A=	NP_001358585.1:p.Gln1034=
NM_001374820.1:c.3101A=	NP_001361749.1:p.Gln1034=
NM_001374828.1:c.3062A= MANE Select	NP_001361757.1:p.Gln1021=
NM_017519.3:c.3062A=	NP_059989.3:p.Gln1021=