Canonical Allele Identifier: CA366241380

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4604G>C	ENSP00000055163.8:p.Trp1535Ser
ENST00000414678.8:c.4673G>C	ENSP00000412835.3:p.Trp1558Ser
ENST00000637015.2:c.4892G>C	ENSP00000489729.2:p.Trp1631Ser
ENST00000346085.10:c.4643G>C	ENSP00000344546.5:p.Trp1548Ser
ENST00000350026.10:c.4355G>C	ENSP00000055163.7:p.Trp1452Ser
ENST00000414678.7:c.2921G>C	ENSP00000412835.2:p.Trp974Ser
ENST00000635849.1:c.2084G>C	ENSP00000490948.1:p.Trp695Ser
ENST00000635957.1:c.1715G>C	ENSP00000490385.1:p.Trp572Ser
ENST00000636227.1:n.3226G>C
ENST00000636254.1:n.683G>C
ENST00000636930.2:c.4763G>C MANE Select	ENSP00000490491.2:p.Trp1588Ser
ENST00000636940.1:n.2760G>C
ENST00000637015.1:c.2131G>C
ENST00000637568.1:c.2045G>C
ENST00000637741.1:n.1429G>C
ENST00000637810.1:c.2105G>C	ENSP00000489636.1:p.Trp702Ser
ENST00000637904.1:c.2264G>C	ENSP00000490550.1:p.Trp755Ser
ENST00000647938.1:c.4394G>C	ENSP00000498155.1:p.Trp1465Ser
ENST00000346085.9:c.4394G>C	ENSP00000344546.4:p.Trp1465Ser
ENST00000350026.9:c.4355G>C	ENSP00000055163.7:p.Trp1452Ser
ENST00000414678.6:c.2921G>C	ENSP00000412835.2:p.Trp974Ser
NM_017519.2:c.4355G>C	NP_059989.2:p.Trp1452Ser
NM_020732.3:c.4394G>C	NP_065783.3:p.Trp1465Ser
XM_005267069.3:c.4514G>C	XP_005267126.2:p.Trp1505Ser
XM_011535984.1:c.3593G>C	XP_011534286.1:p.Trp1198Ser
XM_011535985.1:c.3413G>C	XP_011534287.1:p.Trp1138Ser
XM_011535986.1:c.3173G>C	XP_011534288.1:p.Trp1058Ser
XM_011535987.1:c.2792G>C	XP_011534289.1:p.Trp931Ser
XM_011535988.1:c.1655G>C	XP_011534290.1:p.Trp552Ser
NM_001346813.1:c.4514G>C	NP_001333742.1:p.Trp1505Ser
NM_001363725.1:c.2264G>C	NP_001350654.1:p.Trp755Ser
XM_011535984.2:c.4724G>C	XP_011534286.2:p.Trp1575Ser
XM_011535988.3:c.1655G>C	XP_011534290.1:p.Trp552Ser
XM_017011103.2:c.4625G>C	XP_016866592.1:p.Trp1542Ser
XM_017011104.1:c.4595G>C	XP_016866593.1:p.Trp1532Ser
XM_017011105.2:c.4565G>C	XP_016866594.1:p.Trp1522Ser
XM_017011106.2:c.4436G>C	XP_016866595.1:p.Trp1479Ser
XM_017011107.2:c.4415G>C	XP_016866596.1:p.Trp1472Ser
XR_002956289.1:n.4710G>C
NM_001363725.2:c.2264G>C	NP_001350654.1:p.Trp755Ser
NM_001371656.1:c.4643G>C	NP_001358585.1:p.Trp1548Ser
NM_001374820.1:c.4643G>C	NP_001361749.1:p.Trp1548Ser
NM_001374828.1:c.4763G>C MANE Select	NP_001361757.1:p.Trp1588Ser
NM_017519.3:c.4604G>C	NP_059989.3:p.Trp1535Ser