Canonical Allele Identifier: CA366241498

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

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