Canonical Allele Identifier: CA366241383

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522123G>C (hg19) ; chr6:g.157200989G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200989G>C , CM000668.2:g.157200989G>C	GRCh38
NC_000006.11:g.157522123G>C , CM000668.1:g.157522123G>C	GRCh37
NC_000006.10:g.157563815G>C	NCBI36
NG_032093.1:g.428060G>C
NG_032093.2:g.428060G>C
NG_066624.1:g.429964G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4605G>C	ENSP00000055163.8:p.Trp1535Cys
ENST00000414678.8:c.4674G>C	ENSP00000412835.3:p.Trp1558Cys
ENST00000637015.2:c.4893G>C	ENSP00000489729.2:p.Trp1631Cys
ENST00000346085.10:c.4644G>C	ENSP00000344546.5:p.Trp1548Cys
ENST00000350026.10:c.4356G>C	ENSP00000055163.7:p.Trp1452Cys
ENST00000414678.7:c.2922G>C	ENSP00000412835.2:p.Trp974Cys
ENST00000635849.1:c.2085G>C	ENSP00000490948.1:p.Trp695Cys
ENST00000635957.1:c.1716G>C	ENSP00000490385.1:p.Trp572Cys
ENST00000636227.1:n.3227G>C
ENST00000636254.1:n.684G>C
ENST00000636930.2:c.4764G>C MANE Select	ENSP00000490491.2:p.Trp1588Cys
ENST00000636940.1:n.2761G>C
ENST00000637015.1:c.2132G>C
ENST00000637568.1:c.2046G>C
ENST00000637741.1:n.1430G>C
ENST00000637810.1:c.2106G>C	ENSP00000489636.1:p.Trp702Cys
ENST00000637904.1:c.2265G>C	ENSP00000490550.1:p.Trp755Cys
ENST00000647938.1:c.4395G>C	ENSP00000498155.1:p.Trp1465Cys
ENST00000346085.9:c.4395G>C	ENSP00000344546.4:p.Trp1465Cys
ENST00000350026.9:c.4356G>C	ENSP00000055163.7:p.Trp1452Cys
ENST00000414678.6:c.2922G>C	ENSP00000412835.2:p.Trp974Cys
NM_017519.2:c.4356G>C	NP_059989.2:p.Trp1452Cys
NM_020732.3:c.4395G>C	NP_065783.3:p.Trp1465Cys
XM_005267069.3:c.4515G>C	XP_005267126.2:p.Trp1505Cys
XM_011535984.1:c.3594G>C	XP_011534286.1:p.Trp1198Cys
XM_011535985.1:c.3414G>C	XP_011534287.1:p.Trp1138Cys
XM_011535986.1:c.3174G>C	XP_011534288.1:p.Trp1058Cys
XM_011535987.1:c.2793G>C	XP_011534289.1:p.Trp931Cys
XM_011535988.1:c.1656G>C	XP_011534290.1:p.Trp552Cys
NM_001346813.1:c.4515G>C	NP_001333742.1:p.Trp1505Cys
NM_001363725.1:c.2265G>C	NP_001350654.1:p.Trp755Cys
XM_011535984.2:c.4725G>C	XP_011534286.2:p.Trp1575Cys
XM_011535988.3:c.1656G>C	XP_011534290.1:p.Trp552Cys
XM_017011103.2:c.4626G>C	XP_016866592.1:p.Trp1542Cys
XM_017011104.1:c.4596G>C	XP_016866593.1:p.Trp1532Cys
XM_017011105.2:c.4566G>C	XP_016866594.1:p.Trp1522Cys
XM_017011106.2:c.4437G>C	XP_016866595.1:p.Trp1479Cys
XM_017011107.2:c.4416G>C	XP_016866596.1:p.Trp1472Cys
XR_002956289.1:n.4711G>C
NM_001363725.2:c.2265G>C	NP_001350654.1:p.Trp755Cys
NM_001371656.1:c.4644G>C	NP_001358585.1:p.Trp1548Cys
NM_001374820.1:c.4644G>C	NP_001361749.1:p.Trp1548Cys
NM_001374828.1:c.4764G>C MANE Select	NP_001361757.1:p.Trp1588Cys
NM_017519.3:c.4605G>C	NP_059989.3:p.Trp1535Cys