Canonical Allele Identifier: CA366242511

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128375885
• MyVariant Identifiers: chr6:g.157522454C>A (hg19) ; chr6:g.157201320C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201320C>A , CM000668.2:g.157201320C>A	GRCh38
NC_000006.11:g.157522454C>A , CM000668.1:g.157522454C>A	GRCh37
NC_000006.10:g.157564146C>A	NCBI36
NG_032093.1:g.428391C>A
NG_032093.2:g.428391C>A
NG_066624.1:g.430295C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4936C>A	ENSP00000055163.8:p.Pro1646Thr
ENST00000414678.8:c.5005C>A	ENSP00000412835.3:p.Pro1669Thr
ENST00000637015.2:c.5224C>A	ENSP00000489729.2:p.Pro1742Thr
ENST00000346085.10:c.4975C>A	ENSP00000344546.5:p.Pro1659Thr
ENST00000350026.10:c.4687C>A	ENSP00000055163.7:p.Pro1563Thr
ENST00000414678.7:c.3253C>A	ENSP00000412835.2:p.Pro1085Thr
ENST00000635849.1:c.2416C>A	ENSP00000490948.1:p.Pro806Thr
ENST00000635957.1:c.2047C>A	ENSP00000490385.1:p.Pro683Thr
ENST00000636227.1:n.3558C>A
ENST00000636254.1:n.1015C>A
ENST00000636930.2:c.5095C>A MANE Select	ENSP00000490491.2:p.Pro1699Thr
ENST00000636940.1:n.3092C>A
ENST00000637015.1:c.2463C>A
ENST00000637568.1:c.2377C>A
ENST00000637741.1:n.1761C>A
ENST00000637810.1:c.2437C>A	ENSP00000489636.1:p.Pro813Thr
ENST00000637904.1:c.2596C>A	ENSP00000490550.1:p.Pro866Thr
ENST00000647938.1:c.4726C>A	ENSP00000498155.1:p.Pro1576Thr
ENST00000346085.9:c.4726C>A	ENSP00000344546.4:p.Pro1576Thr
ENST00000350026.9:c.4687C>A	ENSP00000055163.7:p.Pro1563Thr
ENST00000414678.6:c.3253C>A	ENSP00000412835.2:p.Pro1085Thr
NM_017519.2:c.4687C>A	NP_059989.2:p.Pro1563Thr
NM_020732.3:c.4726C>A	NP_065783.3:p.Pro1576Thr
XM_005267069.3:c.4846C>A	XP_005267126.2:p.Pro1616Thr
XM_011535984.1:c.3925C>A	XP_011534286.1:p.Pro1309Thr
XM_011535985.1:c.3745C>A	XP_011534287.1:p.Pro1249Thr
XM_011535986.1:c.3505C>A	XP_011534288.1:p.Pro1169Thr
XM_011535987.1:c.3124C>A	XP_011534289.1:p.Pro1042Thr
XM_011535988.1:c.1987C>A	XP_011534290.1:p.Pro663Thr
NM_001346813.1:c.4846C>A	NP_001333742.1:p.Pro1616Thr
NM_001363725.1:c.2596C>A	NP_001350654.1:p.Pro866Thr
XM_011535984.2:c.5056C>A	XP_011534286.2:p.Pro1686Thr
XM_011535988.3:c.1987C>A	XP_011534290.1:p.Pro663Thr
XM_017011103.2:c.4957C>A	XP_016866592.1:p.Pro1653Thr
XM_017011104.1:c.4927C>A	XP_016866593.1:p.Pro1643Thr
XM_017011105.2:c.4897C>A	XP_016866594.1:p.Pro1633Thr
XM_017011106.2:c.4768C>A	XP_016866595.1:p.Pro1590Thr
XM_017011107.2:c.4747C>A	XP_016866596.1:p.Pro1583Thr
XR_002956289.1:n.5042C>A
NM_001363725.2:c.2596C>A	NP_001350654.1:p.Pro866Thr
NM_001371656.1:c.4975C>A	NP_001358585.1:p.Pro1659Thr
NM_001374820.1:c.4975C>A	NP_001361749.1:p.Pro1659Thr
NM_001374828.1:c.5095C>A MANE Select	NP_001361757.1:p.Pro1699Thr
NM_017519.3:c.4936C>A	NP_059989.3:p.Pro1646Thr