Canonical Allele Identifier: CA366228202

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317574
• MyVariant Identifiers: chr6:g.157502262G>A (hg19) ; chr6:g.157181128G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181128G>A , CM000668.2:g.157181128G>A	GRCh38
NC_000006.11:g.157502262G>A , CM000668.1:g.157502262G>A	GRCh37
NC_000006.10:g.157543954G>A	NCBI36
NG_032093.1:g.408199G>A
NG_032093.2:g.408199G>A
NG_066624.1:g.410103G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3505G>A	ENSP00000055163.8:p.Asp1169Asn
ENST00000414678.8:c.3574G>A	ENSP00000412835.3:p.Asp1192Asn
ENST00000637015.2:c.3793G>A	ENSP00000489729.2:p.Asp1265Asn
ENST00000319584.11:c.1678G>A	ENSP00000313006.7:p.Asp560Asn
ENST00000346085.10:c.3544G>A	ENSP00000344546.5:p.Asp1182Asn
ENST00000350026.10:c.3256G>A	ENSP00000055163.7:p.Asp1086Asn
ENST00000414678.7:c.1822G>A	ENSP00000412835.2:p.Asp608Asn
ENST00000635849.1:c.985G>A	ENSP00000490948.1:p.Asp329Asn
ENST00000635957.1:c.619G>A	ENSP00000490385.1:p.Asp207Asn
ENST00000636930.2:c.3664G>A MANE Select	ENSP00000490491.2:p.Asp1222Asn
ENST00000636940.1:n.1661G>A
ENST00000637015.1:c.1032G>A
ENST00000637568.1:c.946G>A
ENST00000637741.1:n.330G>A
ENST00000637810.1:c.1006G>A	ENSP00000489636.1:p.Asp336Asn
ENST00000637904.1:c.1165G>A	ENSP00000490550.1:p.Asp389Asn
ENST00000647938.1:c.3295G>A	ENSP00000498155.1:p.Asp1099Asn
ENST00000319584.10:c.1681G>A	ENSP00000313006.6:p.Asp561Asn
ENST00000346085.9:c.3295G>A	ENSP00000344546.4:p.Asp1099Asn
ENST00000350026.9:c.3256G>A	ENSP00000055163.7:p.Asp1086Asn
ENST00000400790.3:c.457G>A	ENSP00000383596.3:p.Asp153Asn
ENST00000414678.6:c.1822G>A	ENSP00000412835.2:p.Asp608Asn
ENST00000478761.3:c.866G>A
NM_017519.2:c.3256G>A	NP_059989.2:p.Asp1086Asn
NM_020732.3:c.3295G>A	NP_065783.3:p.Asp1099Asn
XM_005267069.3:c.3415G>A	XP_005267126.2:p.Asp1139Asn
XM_011535984.1:c.2494G>A	XP_011534286.1:p.Asp832Asn
XM_011535985.1:c.2314G>A	XP_011534287.1:p.Asp772Asn
XM_011535986.1:c.2074G>A	XP_011534288.1:p.Asp692Asn
XM_011535987.1:c.1693G>A	XP_011534289.1:p.Asp565Asn
XM_011535988.1:c.556G>A	XP_011534290.1:p.Asp186Asn
NM_001346813.1:c.3415G>A	NP_001333742.1:p.Asp1139Asn
NM_001363725.1:c.1165G>A	NP_001350654.1:p.Asp389Asn
XM_011535984.2:c.3625G>A	XP_011534286.2:p.Asp1209Asn
XM_011535988.3:c.556G>A	XP_011534290.1:p.Asp186Asn
XM_017011103.2:c.3526G>A	XP_016866592.1:p.Asp1176Asn
XM_017011104.1:c.3496G>A	XP_016866593.1:p.Asp1166Asn
XM_017011105.2:c.3466G>A	XP_016866594.1:p.Asp1156Asn
XM_017011106.2:c.3337G>A	XP_016866595.1:p.Asp1113Asn
XM_017011107.2:c.3316G>A	XP_016866596.1:p.Asp1106Asn
XR_002956289.1:n.3708G>A
NM_001363725.2:c.1165G>A	NP_001350654.1:p.Asp389Asn
NM_001371656.1:c.3544G>A	NP_001358585.1:p.Asp1182Asn
NM_001374820.1:c.3544G>A	NP_001361749.1:p.Asp1182Asn
NM_001374828.1:c.3664G>A MANE Select	NP_001361757.1:p.Asp1222Asn
NM_017519.3:c.3505G>A	NP_059989.3:p.Asp1169Asn