Canonical Allele Identifier: CA366241499

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522147T>A (hg19) ; chr6:g.157201013T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201013T>A , CM000668.2:g.157201013T>A	GRCh38
NC_000006.11:g.157522147T>A , CM000668.1:g.157522147T>A	GRCh37
NC_000006.10:g.157563839T>A	NCBI36
NG_032093.1:g.428084T>A
NG_032093.2:g.428084T>A
NG_066624.1:g.429988T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4629T>A	ENSP00000055163.8:p.Tyr1543Ter
ENST00000414678.8:c.4698T>A	ENSP00000412835.3:p.Tyr1566Ter
ENST00000637015.2:c.4917T>A	ENSP00000489729.2:p.Tyr1639Ter
ENST00000346085.10:c.4668T>A	ENSP00000344546.5:p.Tyr1556Ter
ENST00000350026.10:c.4380T>A	ENSP00000055163.7:p.Tyr1460Ter
ENST00000414678.7:c.2946T>A	ENSP00000412835.2:p.Tyr982Ter
ENST00000635849.1:c.2109T>A	ENSP00000490948.1:p.Tyr703Ter
ENST00000635957.1:c.1740T>A	ENSP00000490385.1:p.Tyr580Ter
ENST00000636227.1:n.3251T>A
ENST00000636254.1:n.708T>A
ENST00000636930.2:c.4788T>A MANE Select	ENSP00000490491.2:p.Tyr1596Ter
ENST00000636940.1:n.2785T>A
ENST00000637015.1:c.2156T>A
ENST00000637568.1:c.2070T>A
ENST00000637741.1:n.1454T>A
ENST00000637810.1:c.2130T>A	ENSP00000489636.1:p.Tyr710Ter
ENST00000637904.1:c.2289T>A	ENSP00000490550.1:p.Tyr763Ter
ENST00000647938.1:c.4419T>A	ENSP00000498155.1:p.Tyr1473Ter
ENST00000346085.9:c.4419T>A	ENSP00000344546.4:p.Tyr1473Ter
ENST00000350026.9:c.4380T>A	ENSP00000055163.7:p.Tyr1460Ter
ENST00000414678.6:c.2946T>A	ENSP00000412835.2:p.Tyr982Ter
NM_017519.2:c.4380T>A	NP_059989.2:p.Tyr1460Ter
NM_020732.3:c.4419T>A	NP_065783.3:p.Tyr1473Ter
XM_005267069.3:c.4539T>A	XP_005267126.2:p.Tyr1513Ter
XM_011535984.1:c.3618T>A	XP_011534286.1:p.Tyr1206Ter
XM_011535985.1:c.3438T>A	XP_011534287.1:p.Tyr1146Ter
XM_011535986.1:c.3198T>A	XP_011534288.1:p.Tyr1066Ter
XM_011535987.1:c.2817T>A	XP_011534289.1:p.Tyr939Ter
XM_011535988.1:c.1680T>A	XP_011534290.1:p.Tyr560Ter
NM_001346813.1:c.4539T>A	NP_001333742.1:p.Tyr1513Ter
NM_001363725.1:c.2289T>A	NP_001350654.1:p.Tyr763Ter
XM_011535984.2:c.4749T>A	XP_011534286.2:p.Tyr1583Ter
XM_011535988.3:c.1680T>A	XP_011534290.1:p.Tyr560Ter
XM_017011103.2:c.4650T>A	XP_016866592.1:p.Tyr1550Ter
XM_017011104.1:c.4620T>A	XP_016866593.1:p.Tyr1540Ter
XM_017011105.2:c.4590T>A	XP_016866594.1:p.Tyr1530Ter
XM_017011106.2:c.4461T>A	XP_016866595.1:p.Tyr1487Ter
XM_017011107.2:c.4440T>A	XP_016866596.1:p.Tyr1480Ter
XR_002956289.1:n.4735T>A
NM_001363725.2:c.2289T>A	NP_001350654.1:p.Tyr763Ter
NM_001371656.1:c.4668T>A	NP_001358585.1:p.Tyr1556Ter
NM_001374820.1:c.4668T>A	NP_001361749.1:p.Tyr1556Ter
NM_001374828.1:c.4788T>A MANE Select	NP_001361757.1:p.Tyr1596Ter
NM_017519.3:c.4629T>A	NP_059989.3:p.Tyr1543Ter