Canonical Allele Identifier: CA366239447

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157519947A>C (hg19) ; chr6:g.157198813A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198813A>C , CM000668.2:g.157198813A>C	GRCh38
NC_000006.11:g.157519947A>C , CM000668.1:g.157519947A>C	GRCh37
NC_000006.10:g.157561639A>C	NCBI36
NG_032093.1:g.425884A>C
NG_032093.2:g.425884A>C
NG_066624.1:g.427788A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4226A>C	ENSP00000055163.8:p.His1409Pro
ENST00000414678.8:c.4295A>C	ENSP00000412835.3:p.His1432Pro
ENST00000637015.2:c.4514A>C	ENSP00000489729.2:p.His1505Pro
ENST00000346085.10:c.4265A>C	ENSP00000344546.5:p.His1422Pro
ENST00000350026.10:c.3977A>C	ENSP00000055163.7:p.His1326Pro
ENST00000414678.7:c.2543A>C	ENSP00000412835.2:p.His848Pro
ENST00000635849.1:c.1706A>C	ENSP00000490948.1:p.His569Pro
ENST00000635957.1:c.1337A>C	ENSP00000490385.1:p.His446Pro
ENST00000636227.1:n.2848A>C
ENST00000636254.1:n.305A>C
ENST00000636930.2:c.4385A>C MANE Select	ENSP00000490491.2:p.His1462Pro
ENST00000636940.1:n.2382A>C
ENST00000637015.1:c.1753A>C
ENST00000637568.1:c.1667A>C
ENST00000637741.1:n.1051A>C
ENST00000637810.1:c.1727A>C	ENSP00000489636.1:p.His576Pro
ENST00000637904.1:c.1886A>C	ENSP00000490550.1:p.His629Pro
ENST00000647938.1:c.4016A>C	ENSP00000498155.1:p.His1339Pro
ENST00000346085.9:c.4016A>C	ENSP00000344546.4:p.His1339Pro
ENST00000350026.9:c.3977A>C	ENSP00000055163.7:p.His1326Pro
ENST00000414678.6:c.2543A>C	ENSP00000412835.2:p.His848Pro
NM_017519.2:c.3977A>C	NP_059989.2:p.His1326Pro
NM_020732.3:c.4016A>C	NP_065783.3:p.His1339Pro
XM_005267069.3:c.4136A>C	XP_005267126.2:p.His1379Pro
XM_011535984.1:c.3215A>C	XP_011534286.1:p.His1072Pro
XM_011535985.1:c.3035A>C	XP_011534287.1:p.His1012Pro
XM_011535986.1:c.2795A>C	XP_011534288.1:p.His932Pro
XM_011535987.1:c.2414A>C	XP_011534289.1:p.His805Pro
XM_011535988.1:c.1277A>C	XP_011534290.1:p.His426Pro
NM_001346813.1:c.4136A>C	NP_001333742.1:p.His1379Pro
NM_001363725.1:c.1886A>C	NP_001350654.1:p.His629Pro
XM_011535984.2:c.4346A>C	XP_011534286.2:p.His1449Pro
XM_011535988.3:c.1277A>C	XP_011534290.1:p.His426Pro
XM_017011103.2:c.4247A>C	XP_016866592.1:p.His1416Pro
XM_017011104.1:c.4217A>C	XP_016866593.1:p.His1406Pro
XM_017011105.2:c.4187A>C	XP_016866594.1:p.His1396Pro
XM_017011106.2:c.4058A>C	XP_016866595.1:p.His1353Pro
XM_017011107.2:c.4037A>C	XP_016866596.1:p.His1346Pro
XR_002956289.1:n.4427-1892A>C
NM_001363725.2:c.1886A>C	NP_001350654.1:p.His629Pro
NM_001371656.1:c.4265A>C	NP_001358585.1:p.His1422Pro
NM_001374820.1:c.4265A>C	NP_001361749.1:p.His1422Pro
NM_001374828.1:c.4385A>C MANE Select	NP_001361757.1:p.His1462Pro
NM_017519.3:c.4226A>C	NP_059989.3:p.His1409Pro