Canonical Allele Identifier: CA4067880

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206444C>T , CM000668.2:g.157206444C>T	GRCh38
NC_000006.11:g.157527578C>T , CM000668.1:g.157527578C>T	GRCh37
NC_000006.10:g.157569270C>T	NCBI36
NG_032093.1:g.433515C>T
NG_032093.2:g.433515C>T
NG_066624.1:g.435419C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.5672C>T MANE Select	NP_001361757.1:p.Pro1891Leu
ENST00000636930.2:c.5672C>T MANE Select	ENSP00000490491.2:p.Pro1891Leu
NM_001346813.1:c.5423C>T	NP_001333742.1:p.Pro1808Leu
NM_001363725.1:c.3173C>T	NP_001350654.1:p.Pro1058Leu
NM_001363725.2:c.3173C>T	NP_001350654.1:p.Pro1058Leu
NM_001371656.1:c.5552C>T	NP_001358585.1:p.Pro1851Leu
NM_001374820.1:c.5552C>T	NP_001361749.1:p.Pro1851Leu
NM_017519.2:c.5264C>T	NP_059989.2:p.Pro1755Leu
NM_017519.3:c.5513C>T	NP_059989.3:p.Pro1838Leu
NM_020732.3:c.5303C>T	NP_065783.3:p.Pro1768Leu
ENST00000346085.10:c.5552C>T	ENSP00000344546.5:p.Pro1851Leu
ENST00000346085.9:c.5303C>T	ENSP00000344546.4:p.Pro1768Leu
ENST00000350026.10:c.5264C>T	ENSP00000055163.7:p.Pro1755Leu
ENST00000350026.11:c.5513C>T	ENSP00000055163.8:p.Pro1838Leu
ENST00000350026.9:c.5264C>T	ENSP00000055163.7:p.Pro1755Leu
ENST00000414678.6:c.3830C>T	ENSP00000412835.2:p.Pro1277Leu
ENST00000414678.7:c.3830C>T	ENSP00000412835.2:p.Pro1277Leu
ENST00000414678.8:c.5582C>T	ENSP00000412835.3:p.Pro1861Leu
ENST00000635849.1:c.2993C>T	ENSP00000490948.1:p.Pro998Leu
ENST00000635957.1:c.2624C>T	ENSP00000490385.1:p.Pro875Leu
ENST00000636227.1:n.4135C>T
ENST00000636254.1:n.1592C>T
ENST00000636940.1:n.3669C>T
ENST00000637015.1:c.3040C>T
ENST00000637015.2:c.5801C>T	ENSP00000489729.2:p.Pro1934Leu
ENST00000637568.1:c.2954C>T
ENST00000637741.1:n.2338C>T
ENST00000637810.1:c.3014C>T	ENSP00000489636.1:p.Pro1005Leu
ENST00000637904.1:c.3173C>T	ENSP00000490550.1:p.Pro1058Leu
ENST00000637933.1:n.2787C>T
ENST00000647938.1:c.5303C>T	ENSP00000498155.1:p.Pro1768Leu
XM_005267069.3:c.5423C>T	XP_005267126.2:p.Pro1808Leu
XM_011535984.1:c.4502C>T	XP_011534286.1:p.Pro1501Leu
XM_011535984.2:c.5633C>T	XP_011534286.2:p.Pro1878Leu
XM_011535985.1:c.4322C>T	XP_011534287.1:p.Pro1441Leu
XM_011535986.1:c.4082C>T	XP_011534288.1:p.Pro1361Leu
XM_011535987.1:c.3701C>T	XP_011534289.1:p.Pro1234Leu
XM_011535988.1:c.2564C>T	XP_011534290.1:p.Pro855Leu
XM_011535988.3:c.2564C>T	XP_011534290.1:p.Pro855Leu
XM_017011103.2:c.5534C>T	XP_016866592.1:p.Pro1845Leu
XM_017011104.1:c.5504C>T	XP_016866593.1:p.Pro1835Leu
XM_017011105.2:c.5474C>T	XP_016866594.1:p.Pro1825Leu
XM_017011106.2:c.5345C>T	XP_016866595.1:p.Pro1782Leu
XM_017011107.2:c.5324C>T	XP_016866596.1:p.Pro1775Leu
XR_002956289.1:n.5619C>T