Canonical Allele Identifier: CA366241584

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522161G>C (hg19) ; chr6:g.157201027G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201027G>C , CM000668.2:g.157201027G>C	GRCh38
NC_000006.11:g.157522161G>C , CM000668.1:g.157522161G>C	GRCh37
NC_000006.10:g.157563853G>C	NCBI36
NG_032093.1:g.428098G>C
NG_032093.2:g.428098G>C
NG_066624.1:g.430002G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4643G>C	ENSP00000055163.8:p.Arg1548Thr
ENST00000414678.8:c.4712G>C	ENSP00000412835.3:p.Arg1571Thr
ENST00000637015.2:c.4931G>C	ENSP00000489729.2:p.Arg1644Thr
ENST00000346085.10:c.4682G>C	ENSP00000344546.5:p.Arg1561Thr
ENST00000350026.10:c.4394G>C	ENSP00000055163.7:p.Arg1465Thr
ENST00000414678.7:c.2960G>C	ENSP00000412835.2:p.Arg987Thr
ENST00000635849.1:c.2123G>C	ENSP00000490948.1:p.Arg708Thr
ENST00000635957.1:c.1754G>C	ENSP00000490385.1:p.Arg585Thr
ENST00000636227.1:n.3265G>C
ENST00000636254.1:n.722G>C
ENST00000636930.2:c.4802G>C MANE Select	ENSP00000490491.2:p.Arg1601Thr
ENST00000636940.1:n.2799G>C
ENST00000637015.1:c.2170G>C
ENST00000637568.1:c.2084G>C
ENST00000637741.1:n.1468G>C
ENST00000637810.1:c.2144G>C	ENSP00000489636.1:p.Arg715Thr
ENST00000637904.1:c.2303G>C	ENSP00000490550.1:p.Arg768Thr
ENST00000647938.1:c.4433G>C	ENSP00000498155.1:p.Arg1478Thr
ENST00000346085.9:c.4433G>C	ENSP00000344546.4:p.Arg1478Thr
ENST00000350026.9:c.4394G>C	ENSP00000055163.7:p.Arg1465Thr
ENST00000414678.6:c.2960G>C	ENSP00000412835.2:p.Arg987Thr
NM_017519.2:c.4394G>C	NP_059989.2:p.Arg1465Thr
NM_020732.3:c.4433G>C	NP_065783.3:p.Arg1478Thr
XM_005267069.3:c.4553G>C	XP_005267126.2:p.Arg1518Thr
XM_011535984.1:c.3632G>C	XP_011534286.1:p.Arg1211Thr
XM_011535985.1:c.3452G>C	XP_011534287.1:p.Arg1151Thr
XM_011535986.1:c.3212G>C	XP_011534288.1:p.Arg1071Thr
XM_011535987.1:c.2831G>C	XP_011534289.1:p.Arg944Thr
XM_011535988.1:c.1694G>C	XP_011534290.1:p.Arg565Thr
NM_001346813.1:c.4553G>C	NP_001333742.1:p.Arg1518Thr
NM_001363725.1:c.2303G>C	NP_001350654.1:p.Arg768Thr
XM_011535984.2:c.4763G>C	XP_011534286.2:p.Arg1588Thr
XM_011535988.3:c.1694G>C	XP_011534290.1:p.Arg565Thr
XM_017011103.2:c.4664G>C	XP_016866592.1:p.Arg1555Thr
XM_017011104.1:c.4634G>C	XP_016866593.1:p.Arg1545Thr
XM_017011105.2:c.4604G>C	XP_016866594.1:p.Arg1535Thr
XM_017011106.2:c.4475G>C	XP_016866595.1:p.Arg1492Thr
XM_017011107.2:c.4454G>C	XP_016866596.1:p.Arg1485Thr
XR_002956289.1:n.4749G>C
NM_001363725.2:c.2303G>C	NP_001350654.1:p.Arg768Thr
NM_001371656.1:c.4682G>C	NP_001358585.1:p.Arg1561Thr
NM_001374820.1:c.4682G>C	NP_001361749.1:p.Arg1561Thr
NM_001374828.1:c.4802G>C MANE Select	NP_001361757.1:p.Arg1601Thr
NM_017519.3:c.4643G>C	NP_059989.3:p.Arg1548Thr