Canonical Allele Identifier: CA366227535

Gene: ARID1B

Linked Data

• COSMIC: COSM4910979 ; COSM4910980
• MyVariant Identifiers: chr6:g.157502181T>A (hg19) ; chr6:g.157181047T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181047T>A , CM000668.2:g.157181047T>A	GRCh38
NC_000006.11:g.157502181T>A , CM000668.1:g.157502181T>A	GRCh37
NC_000006.10:g.157543873T>A	NCBI36
NG_032093.1:g.408118T>A
NG_032093.2:g.408118T>A
NG_066624.1:g.410022T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3424T>A	ENSP00000055163.8:p.Trp1142Arg
ENST00000414678.8:c.3493T>A	ENSP00000412835.3:p.Trp1165Arg
ENST00000637015.2:c.3712T>A	ENSP00000489729.2:p.Trp1238Arg
ENST00000319584.11:c.1597T>A	ENSP00000313006.7:p.Trp533Arg
ENST00000346085.10:c.3463T>A	ENSP00000344546.5:p.Trp1155Arg
ENST00000350026.10:c.3175T>A	ENSP00000055163.7:p.Trp1059Arg
ENST00000414678.7:c.1741T>A	ENSP00000412835.2:p.Trp581Arg
ENST00000635849.1:c.904T>A	ENSP00000490948.1:p.Trp302Arg
ENST00000635957.1:c.538T>A	ENSP00000490385.1:p.Trp180Arg
ENST00000636930.2:c.3583T>A MANE Select	ENSP00000490491.2:p.Trp1195Arg
ENST00000636940.1:n.1580T>A
ENST00000637015.1:c.951T>A
ENST00000637568.1:c.865T>A
ENST00000637741.1:n.249T>A
ENST00000637810.1:c.925T>A	ENSP00000489636.1:p.Trp309Arg
ENST00000637904.1:c.1084T>A	ENSP00000490550.1:p.Trp362Arg
ENST00000647938.1:c.3214T>A	ENSP00000498155.1:p.Trp1072Arg
ENST00000319584.10:c.1600T>A	ENSP00000313006.6:p.Trp534Arg
ENST00000346085.9:c.3214T>A	ENSP00000344546.4:p.Trp1072Arg
ENST00000350026.9:c.3175T>A	ENSP00000055163.7:p.Trp1059Arg
ENST00000400790.3:c.376T>A	ENSP00000383596.3:p.Trp126Arg
ENST00000414678.6:c.1741T>A	ENSP00000412835.2:p.Trp581Arg
ENST00000478761.3:c.785T>A
NM_017519.2:c.3175T>A	NP_059989.2:p.Trp1059Arg
NM_020732.3:c.3214T>A	NP_065783.3:p.Trp1072Arg
XM_005267069.3:c.3334T>A	XP_005267126.2:p.Trp1112Arg
XM_011535984.1:c.2413T>A	XP_011534286.1:p.Trp805Arg
XM_011535985.1:c.2233T>A	XP_011534287.1:p.Trp745Arg
XM_011535986.1:c.1993T>A	XP_011534288.1:p.Trp665Arg
XM_011535987.1:c.1612T>A	XP_011534289.1:p.Trp538Arg
XM_011535988.1:c.475T>A	XP_011534290.1:p.Trp159Arg
NM_001346813.1:c.3334T>A	NP_001333742.1:p.Trp1112Arg
NM_001363725.1:c.1084T>A	NP_001350654.1:p.Trp362Arg
XM_011535984.2:c.3544T>A	XP_011534286.2:p.Trp1182Arg
XM_011535988.3:c.475T>A	XP_011534290.1:p.Trp159Arg
XM_017011103.2:c.3445T>A	XP_016866592.1:p.Trp1149Arg
XM_017011104.1:c.3415T>A	XP_016866593.1:p.Trp1139Arg
XM_017011105.2:c.3385T>A	XP_016866594.1:p.Trp1129Arg
XM_017011106.2:c.3256T>A	XP_016866595.1:p.Trp1086Arg
XM_017011107.2:c.3235T>A	XP_016866596.1:p.Trp1079Arg
XR_002956289.1:n.3627T>A
NM_001363725.2:c.1084T>A	NP_001350654.1:p.Trp362Arg
NM_001371656.1:c.3463T>A	NP_001358585.1:p.Trp1155Arg
NM_001374820.1:c.3463T>A	NP_001361749.1:p.Trp1155Arg
NM_001374828.1:c.3583T>A MANE Select	NP_001361757.1:p.Trp1195Arg
NM_017519.3:c.3424T>A	NP_059989.3:p.Trp1142Arg