Canonical Allele Identifier: CA366234958

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511207A>T (hg19) ; chr6:g.157190073A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190073A>T , CM000668.2:g.157190073A>T	GRCh38
NC_000006.11:g.157511207A>T , CM000668.1:g.157511207A>T	GRCh37
NC_000006.10:g.157552899A>T	NCBI36
NG_032093.1:g.417144A>T
NG_032093.2:g.417144A>T
NG_066624.1:g.419048A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3935A>T	ENSP00000055163.8:p.Asp1312Val
ENST00000414678.8:c.4004A>T	ENSP00000412835.3:p.Asp1335Val
ENST00000637015.2:c.4223A>T	ENSP00000489729.2:p.Asp1408Val
ENST00000346085.10:c.3974A>T	ENSP00000344546.5:p.Asp1325Val
ENST00000350026.10:c.3686A>T	ENSP00000055163.7:p.Asp1229Val
ENST00000414678.7:c.2252A>T	ENSP00000412835.2:p.Asp751Val
ENST00000635849.1:c.1415A>T	ENSP00000490948.1:p.Asp472Val
ENST00000635957.1:c.1046A>T	ENSP00000490385.1:p.Asp349Val
ENST00000636930.2:c.4094A>T MANE Select	ENSP00000490491.2:p.Asp1365Val
ENST00000636940.1:n.2091A>T
ENST00000637015.1:c.1462A>T
ENST00000637568.1:c.1376A>T
ENST00000637741.1:n.760A>T
ENST00000637810.1:c.1436A>T	ENSP00000489636.1:p.Asp479Val
ENST00000637904.1:c.1595A>T	ENSP00000490550.1:p.Asp532Val
ENST00000647938.1:c.3725A>T	ENSP00000498155.1:p.Asp1242Val
ENST00000346085.9:c.3725A>T	ENSP00000344546.4:p.Asp1242Val
ENST00000350026.9:c.3686A>T	ENSP00000055163.7:p.Asp1229Val
ENST00000414678.6:c.2252A>T	ENSP00000412835.2:p.Asp751Val
NM_017519.2:c.3686A>T	NP_059989.2:p.Asp1229Val
NM_020732.3:c.3725A>T	NP_065783.3:p.Asp1242Val
XM_005267069.3:c.3845A>T	XP_005267126.2:p.Asp1282Val
XM_011535984.1:c.2924A>T	XP_011534286.1:p.Asp975Val
XM_011535985.1:c.2744A>T	XP_011534287.1:p.Asp915Val
XM_011535986.1:c.2504A>T	XP_011534288.1:p.Asp835Val
XM_011535987.1:c.2123A>T	XP_011534289.1:p.Asp708Val
XM_011535988.1:c.986A>T	XP_011534290.1:p.Asp329Val
NM_001346813.1:c.3845A>T	NP_001333742.1:p.Asp1282Val
NM_001363725.1:c.1595A>T	NP_001350654.1:p.Asp532Val
XM_011535984.2:c.4055A>T	XP_011534286.2:p.Asp1352Val
XM_011535988.3:c.986A>T	XP_011534290.1:p.Asp329Val
XM_017011103.2:c.3956A>T	XP_016866592.1:p.Asp1319Val
XM_017011104.1:c.3926A>T	XP_016866593.1:p.Asp1309Val
XM_017011105.2:c.3896A>T	XP_016866594.1:p.Asp1299Val
XM_017011106.2:c.3767A>T	XP_016866595.1:p.Asp1256Val
XM_017011107.2:c.3746A>T	XP_016866596.1:p.Asp1249Val
XR_002956289.1:n.4138A>T
NM_001363725.2:c.1595A>T	NP_001350654.1:p.Asp532Val
NM_001371656.1:c.3974A>T	NP_001358585.1:p.Asp1325Val
NM_001374820.1:c.3974A>T	NP_001361749.1:p.Asp1325Val
NM_001374828.1:c.4094A>T MANE Select	NP_001361757.1:p.Asp1365Val
NM_017519.3:c.3935A>T	NP_059989.3:p.Asp1312Val