Canonical Allele Identifier: CA366234952

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511206G>T (hg19) ; chr6:g.157190072G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190072G>T , CM000668.2:g.157190072G>T	GRCh38
NC_000006.11:g.157511206G>T , CM000668.1:g.157511206G>T	GRCh37
NC_000006.10:g.157552898G>T	NCBI36
NG_032093.1:g.417143G>T
NG_032093.2:g.417143G>T
NG_066624.1:g.419047G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3934G>T	ENSP00000055163.8:p.Asp1312Tyr
ENST00000414678.8:c.4003G>T	ENSP00000412835.3:p.Asp1335Tyr
ENST00000637015.2:c.4222G>T	ENSP00000489729.2:p.Asp1408Tyr
ENST00000346085.10:c.3973G>T	ENSP00000344546.5:p.Asp1325Tyr
ENST00000350026.10:c.3685G>T	ENSP00000055163.7:p.Asp1229Tyr
ENST00000414678.7:c.2251G>T	ENSP00000412835.2:p.Asp751Tyr
ENST00000635849.1:c.1414G>T	ENSP00000490948.1:p.Asp472Tyr
ENST00000635957.1:c.1045G>T	ENSP00000490385.1:p.Asp349Tyr
ENST00000636930.2:c.4093G>T MANE Select	ENSP00000490491.2:p.Asp1365Tyr
ENST00000636940.1:n.2090G>T
ENST00000637015.1:c.1461G>T
ENST00000637568.1:c.1375G>T
ENST00000637741.1:n.759G>T
ENST00000637810.1:c.1435G>T	ENSP00000489636.1:p.Asp479Tyr
ENST00000637904.1:c.1594G>T	ENSP00000490550.1:p.Asp532Tyr
ENST00000647938.1:c.3724G>T	ENSP00000498155.1:p.Asp1242Tyr
ENST00000346085.9:c.3724G>T	ENSP00000344546.4:p.Asp1242Tyr
ENST00000350026.9:c.3685G>T	ENSP00000055163.7:p.Asp1229Tyr
ENST00000414678.6:c.2251G>T	ENSP00000412835.2:p.Asp751Tyr
NM_017519.2:c.3685G>T	NP_059989.2:p.Asp1229Tyr
NM_020732.3:c.3724G>T	NP_065783.3:p.Asp1242Tyr
XM_005267069.3:c.3844G>T	XP_005267126.2:p.Asp1282Tyr
XM_011535984.1:c.2923G>T	XP_011534286.1:p.Asp975Tyr
XM_011535985.1:c.2743G>T	XP_011534287.1:p.Asp915Tyr
XM_011535986.1:c.2503G>T	XP_011534288.1:p.Asp835Tyr
XM_011535987.1:c.2122G>T	XP_011534289.1:p.Asp708Tyr
XM_011535988.1:c.985G>T	XP_011534290.1:p.Asp329Tyr
NM_001346813.1:c.3844G>T	NP_001333742.1:p.Asp1282Tyr
NM_001363725.1:c.1594G>T	NP_001350654.1:p.Asp532Tyr
XM_011535984.2:c.4054G>T	XP_011534286.2:p.Asp1352Tyr
XM_011535988.3:c.985G>T	XP_011534290.1:p.Asp329Tyr
XM_017011103.2:c.3955G>T	XP_016866592.1:p.Asp1319Tyr
XM_017011104.1:c.3925G>T	XP_016866593.1:p.Asp1309Tyr
XM_017011105.2:c.3895G>T	XP_016866594.1:p.Asp1299Tyr
XM_017011106.2:c.3766G>T	XP_016866595.1:p.Asp1256Tyr
XM_017011107.2:c.3745G>T	XP_016866596.1:p.Asp1249Tyr
XR_002956289.1:n.4137G>T
NM_001363725.2:c.1594G>T	NP_001350654.1:p.Asp532Tyr
NM_001371656.1:c.3973G>T	NP_001358585.1:p.Asp1325Tyr
NM_001374820.1:c.3973G>T	NP_001361749.1:p.Asp1325Tyr
NM_001374828.1:c.4093G>T MANE Select	NP_001361757.1:p.Asp1365Tyr
NM_017519.3:c.3934G>T	NP_059989.3:p.Asp1312Tyr