Canonical Allele Identifier: CA366228192

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502262G>T (hg19) ; chr6:g.157181128G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3505G>T	ENSP00000055163.8:p.Asp1169Tyr
ENST00000414678.8:c.3574G>T	ENSP00000412835.3:p.Asp1192Tyr
ENST00000637015.2:c.3793G>T	ENSP00000489729.2:p.Asp1265Tyr
ENST00000319584.11:c.1678G>T	ENSP00000313006.7:p.Asp560Tyr
ENST00000346085.10:c.3544G>T	ENSP00000344546.5:p.Asp1182Tyr
ENST00000350026.10:c.3256G>T	ENSP00000055163.7:p.Asp1086Tyr
ENST00000414678.7:c.1822G>T	ENSP00000412835.2:p.Asp608Tyr
ENST00000635849.1:c.985G>T	ENSP00000490948.1:p.Asp329Tyr
ENST00000635957.1:c.619G>T	ENSP00000490385.1:p.Asp207Tyr
ENST00000636930.2:c.3664G>T MANE Select	ENSP00000490491.2:p.Asp1222Tyr
ENST00000636940.1:n.1661G>T
ENST00000637015.1:c.1032G>T
ENST00000637568.1:c.946G>T
ENST00000637741.1:n.330G>T
ENST00000637810.1:c.1006G>T	ENSP00000489636.1:p.Asp336Tyr
ENST00000637904.1:c.1165G>T	ENSP00000490550.1:p.Asp389Tyr
ENST00000647938.1:c.3295G>T	ENSP00000498155.1:p.Asp1099Tyr
ENST00000319584.10:c.1681G>T	ENSP00000313006.6:p.Asp561Tyr
ENST00000346085.9:c.3295G>T	ENSP00000344546.4:p.Asp1099Tyr
ENST00000350026.9:c.3256G>T	ENSP00000055163.7:p.Asp1086Tyr
ENST00000400790.3:c.457G>T	ENSP00000383596.3:p.Asp153Tyr
ENST00000414678.6:c.1822G>T	ENSP00000412835.2:p.Asp608Tyr
ENST00000478761.3:c.866G>T
NM_017519.2:c.3256G>T	NP_059989.2:p.Asp1086Tyr
NM_020732.3:c.3295G>T	NP_065783.3:p.Asp1099Tyr
XM_005267069.3:c.3415G>T	XP_005267126.2:p.Asp1139Tyr
XM_011535984.1:c.2494G>T	XP_011534286.1:p.Asp832Tyr
XM_011535985.1:c.2314G>T	XP_011534287.1:p.Asp772Tyr
XM_011535986.1:c.2074G>T	XP_011534288.1:p.Asp692Tyr
XM_011535987.1:c.1693G>T	XP_011534289.1:p.Asp565Tyr
XM_011535988.1:c.556G>T	XP_011534290.1:p.Asp186Tyr
NM_001346813.1:c.3415G>T	NP_001333742.1:p.Asp1139Tyr
NM_001363725.1:c.1165G>T	NP_001350654.1:p.Asp389Tyr
XM_011535984.2:c.3625G>T	XP_011534286.2:p.Asp1209Tyr
XM_011535988.3:c.556G>T	XP_011534290.1:p.Asp186Tyr
XM_017011103.2:c.3526G>T	XP_016866592.1:p.Asp1176Tyr
XM_017011104.1:c.3496G>T	XP_016866593.1:p.Asp1166Tyr
XM_017011105.2:c.3466G>T	XP_016866594.1:p.Asp1156Tyr
XM_017011106.2:c.3337G>T	XP_016866595.1:p.Asp1113Tyr
XM_017011107.2:c.3316G>T	XP_016866596.1:p.Asp1106Tyr
XR_002956289.1:n.3708G>T
NM_001363725.2:c.1165G>T	NP_001350654.1:p.Asp389Tyr
NM_001371656.1:c.3544G>T	NP_001358585.1:p.Asp1182Tyr
NM_001374820.1:c.3544G>T	NP_001361749.1:p.Asp1182Tyr
NM_001374828.1:c.3664G>T MANE Select	NP_001361757.1:p.Asp1222Tyr
NM_017519.3:c.3505G>T	NP_059989.3:p.Asp1169Tyr