Canonical Allele Identifier: CA366241381

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522122G>T (hg19) ; chr6:g.157200988G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200988G>T , CM000668.2:g.157200988G>T	GRCh38
NC_000006.11:g.157522122G>T , CM000668.1:g.157522122G>T	GRCh37
NC_000006.10:g.157563814G>T	NCBI36
NG_032093.1:g.428059G>T
NG_032093.2:g.428059G>T
NG_066624.1:g.429963G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4604G>T	ENSP00000055163.8:p.Trp1535Leu
ENST00000414678.8:c.4673G>T	ENSP00000412835.3:p.Trp1558Leu
ENST00000637015.2:c.4892G>T	ENSP00000489729.2:p.Trp1631Leu
ENST00000346085.10:c.4643G>T	ENSP00000344546.5:p.Trp1548Leu
ENST00000350026.10:c.4355G>T	ENSP00000055163.7:p.Trp1452Leu
ENST00000414678.7:c.2921G>T	ENSP00000412835.2:p.Trp974Leu
ENST00000635849.1:c.2084G>T	ENSP00000490948.1:p.Trp695Leu
ENST00000635957.1:c.1715G>T	ENSP00000490385.1:p.Trp572Leu
ENST00000636227.1:n.3226G>T
ENST00000636254.1:n.683G>T
ENST00000636930.2:c.4763G>T MANE Select	ENSP00000490491.2:p.Trp1588Leu
ENST00000636940.1:n.2760G>T
ENST00000637015.1:c.2131G>T
ENST00000637568.1:c.2045G>T
ENST00000637741.1:n.1429G>T
ENST00000637810.1:c.2105G>T	ENSP00000489636.1:p.Trp702Leu
ENST00000637904.1:c.2264G>T	ENSP00000490550.1:p.Trp755Leu
ENST00000647938.1:c.4394G>T	ENSP00000498155.1:p.Trp1465Leu
ENST00000346085.9:c.4394G>T	ENSP00000344546.4:p.Trp1465Leu
ENST00000350026.9:c.4355G>T	ENSP00000055163.7:p.Trp1452Leu
ENST00000414678.6:c.2921G>T	ENSP00000412835.2:p.Trp974Leu
NM_017519.2:c.4355G>T	NP_059989.2:p.Trp1452Leu
NM_020732.3:c.4394G>T	NP_065783.3:p.Trp1465Leu
XM_005267069.3:c.4514G>T	XP_005267126.2:p.Trp1505Leu
XM_011535984.1:c.3593G>T	XP_011534286.1:p.Trp1198Leu
XM_011535985.1:c.3413G>T	XP_011534287.1:p.Trp1138Leu
XM_011535986.1:c.3173G>T	XP_011534288.1:p.Trp1058Leu
XM_011535987.1:c.2792G>T	XP_011534289.1:p.Trp931Leu
XM_011535988.1:c.1655G>T	XP_011534290.1:p.Trp552Leu
NM_001346813.1:c.4514G>T	NP_001333742.1:p.Trp1505Leu
NM_001363725.1:c.2264G>T	NP_001350654.1:p.Trp755Leu
XM_011535984.2:c.4724G>T	XP_011534286.2:p.Trp1575Leu
XM_011535988.3:c.1655G>T	XP_011534290.1:p.Trp552Leu
XM_017011103.2:c.4625G>T	XP_016866592.1:p.Trp1542Leu
XM_017011104.1:c.4595G>T	XP_016866593.1:p.Trp1532Leu
XM_017011105.2:c.4565G>T	XP_016866594.1:p.Trp1522Leu
XM_017011106.2:c.4436G>T	XP_016866595.1:p.Trp1479Leu
XM_017011107.2:c.4415G>T	XP_016866596.1:p.Trp1472Leu
XR_002956289.1:n.4710G>T
NM_001363725.2:c.2264G>T	NP_001350654.1:p.Trp755Leu
NM_001371656.1:c.4643G>T	NP_001358585.1:p.Trp1548Leu
NM_001374820.1:c.4643G>T	NP_001361749.1:p.Trp1548Leu
NM_001374828.1:c.4763G>T MANE Select	NP_001361757.1:p.Trp1588Leu
NM_017519.3:c.4604G>T	NP_059989.3:p.Trp1535Leu