Canonical Allele Identifier: CA1675516963

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148633C= , CM000668.2:g.157148633C=	GRCh38
NC_000006.11:g.157469767C= , CM000668.1:g.157469767C=	GRCh37
NC_000006.10:g.157511459C=	NCBI36
NG_032093.1:g.375704C=
NG_032093.2:g.375704C=
NG_066624.1:g.377608C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2771C=	ENSP00000055163.8:p.Ser924=
ENST00000414678.8:c.2681C=	ENSP00000412835.3:p.Ser894=
ENST00000637015.2:c.2771C=	ENSP00000489729.2:p.Ser924=
ENST00000319584.11:c.785C=	ENSP00000313006.7:p.Ser262=
ENST00000346085.10:c.2810C=	ENSP00000344546.5:p.Ser937=
ENST00000350026.10:c.2522C=	ENSP00000055163.7:p.Ser841=
ENST00000414678.7:c.929C=	ENSP00000412835.2:p.Ser310=
ENST00000452544.2:n.672C=
ENST00000635849.1:c.92C=	ENSP00000490948.1:p.Ser31=
ENST00000636930.2:c.2771C= MANE Select	ENSP00000490491.2:p.Ser924=
ENST00000637015.1:c.10C=
ENST00000637810.1:c.272C=	ENSP00000489636.1:p.Ser91=
ENST00000637904.1:c.272C=	ENSP00000490550.1:p.Ser91=
ENST00000647938.1:c.2561C=	ENSP00000498155.1:p.Ser854=
ENST00000674190.1:n.1520C=
ENST00000319584.10:c.788C=	ENSP00000313006.6:p.Ser263=
ENST00000346085.9:c.2561C=	ENSP00000344546.4:p.Ser854=
ENST00000350026.9:c.2522C=	ENSP00000055163.7:p.Ser841=
ENST00000414678.6:c.929C=	ENSP00000412835.2:p.Ser310=
ENST00000452544.1:n.618C=
NM_017519.2:c.2522C=	NP_059989.2:p.Ser841=
NM_020732.3:c.2561C=	NP_065783.3:p.Ser854=
XM_005267069.3:c.2522C=	XP_005267126.2:p.Ser841=
XM_011535984.1:c.1472C=	XP_011534286.1:p.Ser491=
XM_011535985.1:c.1292C=	XP_011534287.1:p.Ser431=
XM_011535986.1:c.1052C=	XP_011534288.1:p.Ser351=
XM_011535987.1:c.671C=	XP_011534289.1:p.Ser224=
XM_011535988.1:c.-20+15426C=	XP_011534290.1:n.-20+15426C=
NM_001346813.1:c.2522C=	NP_001333742.1:p.Ser841=
NM_001363725.1:c.272C=	NP_001350654.1:p.Ser91=
XM_011535984.2:c.2603C=	XP_011534286.2:p.Ser868=
XM_011535988.3:c.-20+15426C=	XP_011534290.1:n.-20+15426C=
XM_017011103.2:c.2603C=	XP_016866592.1:p.Ser868=
XM_017011104.1:c.2603C=	XP_016866593.1:p.Ser868=
XM_017011105.2:c.2603C=	XP_016866594.1:p.Ser868=
XM_017011106.2:c.2603C=	XP_016866595.1:p.Ser868=
XM_017011107.2:c.2423C=	XP_016866596.1:p.Ser808=
XR_002956289.1:n.2686C=
NM_001363725.2:c.272C=	NP_001350654.1:p.Ser91=
NM_001371656.1:c.2810C=	NP_001358585.1:p.Ser937=
NM_001374820.1:c.2810C=	NP_001361749.1:p.Ser937=
NM_001374828.1:c.2771C= MANE Select	NP_001361757.1:p.Ser924=
NM_017519.3:c.2771C=	NP_059989.3:p.Ser924=