Canonical Allele Identifier: CA1675523483

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201357C= , CM000668.2:g.157201357C=	GRCh38
NC_000006.11:g.157522491C= , CM000668.1:g.157522491C=	GRCh37
NC_000006.10:g.157564183C=	NCBI36
NG_032093.1:g.428428C=
NG_032093.2:g.428428C=
NG_066624.1:g.430332C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4973C=	ENSP00000055163.8:p.Pro1658=
ENST00000414678.8:c.5042C=	ENSP00000412835.3:p.Pro1681=
ENST00000637015.2:c.5261C=	ENSP00000489729.2:p.Pro1754=
ENST00000346085.10:c.5012C=	ENSP00000344546.5:p.Pro1671=
ENST00000350026.10:c.4724C=	ENSP00000055163.7:p.Pro1575=
ENST00000414678.7:c.3290C=	ENSP00000412835.2:p.Pro1097=
ENST00000635849.1:c.2453C=	ENSP00000490948.1:p.Pro818=
ENST00000635957.1:c.2084C=	ENSP00000490385.1:p.Pro695=
ENST00000636227.1:n.3595C=
ENST00000636254.1:n.1052C=
ENST00000636930.2:c.5132C= MANE Select	ENSP00000490491.2:p.Pro1711=
ENST00000636940.1:n.3129C=
ENST00000637015.1:c.2500C=
ENST00000637568.1:c.2414C=
ENST00000637741.1:n.1798C=
ENST00000637810.1:c.2474C=	ENSP00000489636.1:p.Pro825=
ENST00000637904.1:c.2633C=	ENSP00000490550.1:p.Pro878=
ENST00000647938.1:c.4763C=	ENSP00000498155.1:p.Pro1588=
ENST00000346085.9:c.4763C=	ENSP00000344546.4:p.Pro1588=
ENST00000350026.9:c.4724C=	ENSP00000055163.7:p.Pro1575=
ENST00000414678.6:c.3290C=	ENSP00000412835.2:p.Pro1097=
NM_017519.2:c.4724C=	NP_059989.2:p.Pro1575=
NM_020732.3:c.4763C=	NP_065783.3:p.Pro1588=
XM_005267069.3:c.4883C=	XP_005267126.2:p.Pro1628=
XM_011535984.1:c.3962C=	XP_011534286.1:p.Pro1321=
XM_011535985.1:c.3782C=	XP_011534287.1:p.Pro1261=
XM_011535986.1:c.3542C=	XP_011534288.1:p.Pro1181=
XM_011535987.1:c.3161C=	XP_011534289.1:p.Pro1054=
XM_011535988.1:c.2024C=	XP_011534290.1:p.Pro675=
NM_001346813.1:c.4883C=	NP_001333742.1:p.Pro1628=
NM_001363725.1:c.2633C=	NP_001350654.1:p.Pro878=
XM_011535984.2:c.5093C=	XP_011534286.2:p.Pro1698=
XM_011535988.3:c.2024C=	XP_011534290.1:p.Pro675=
XM_017011103.2:c.4994C=	XP_016866592.1:p.Pro1665=
XM_017011104.1:c.4964C=	XP_016866593.1:p.Pro1655=
XM_017011105.2:c.4934C=	XP_016866594.1:p.Pro1645=
XM_017011106.2:c.4805C=	XP_016866595.1:p.Pro1602=
XM_017011107.2:c.4784C=	XP_016866596.1:p.Pro1595=
XR_002956289.1:n.5079C=
NM_001363725.2:c.2633C=	NP_001350654.1:p.Pro878=
NM_001371656.1:c.5012C=	NP_001358585.1:p.Pro1671=
NM_001374820.1:c.5012C=	NP_001361749.1:p.Pro1671=
NM_001374828.1:c.5132C= MANE Select	NP_001361757.1:p.Pro1711=
NM_017519.3:c.4973C=	NP_059989.3:p.Pro1658=