Canonical Allele Identifier: CA366241116

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522004C>G (hg19) ; chr6:g.157200870C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200870C>G , CM000668.2:g.157200870C>G	GRCh38
NC_000006.11:g.157522004C>G , CM000668.1:g.157522004C>G	GRCh37
NC_000006.10:g.157563696C>G	NCBI36
NG_032093.1:g.427941C>G
NG_032093.2:g.427941C>G
NG_066624.1:g.429845C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4486C>G	ENSP00000055163.8:p.Pro1496Ala
ENST00000414678.8:c.4555C>G	ENSP00000412835.3:p.Pro1519Ala
ENST00000637015.2:c.4774C>G	ENSP00000489729.2:p.Pro1592Ala
ENST00000346085.10:c.4525C>G	ENSP00000344546.5:p.Pro1509Ala
ENST00000350026.10:c.4237C>G	ENSP00000055163.7:p.Pro1413Ala
ENST00000414678.7:c.2803C>G	ENSP00000412835.2:p.Pro935Ala
ENST00000635849.1:c.1966C>G	ENSP00000490948.1:p.Pro656Ala
ENST00000635957.1:c.1597C>G	ENSP00000490385.1:p.Pro533Ala
ENST00000636227.1:n.3108C>G
ENST00000636254.1:n.565C>G
ENST00000636930.2:c.4645C>G MANE Select	ENSP00000490491.2:p.Pro1549Ala
ENST00000636940.1:n.2642C>G
ENST00000637015.1:c.2013C>G
ENST00000637568.1:c.1927C>G
ENST00000637741.1:n.1311C>G
ENST00000637810.1:c.1987C>G	ENSP00000489636.1:p.Pro663Ala
ENST00000637904.1:c.2146C>G	ENSP00000490550.1:p.Pro716Ala
ENST00000647938.1:c.4276C>G	ENSP00000498155.1:p.Pro1426Ala
ENST00000346085.9:c.4276C>G	ENSP00000344546.4:p.Pro1426Ala
ENST00000350026.9:c.4237C>G	ENSP00000055163.7:p.Pro1413Ala
ENST00000414678.6:c.2803C>G	ENSP00000412835.2:p.Pro935Ala
NM_017519.2:c.4237C>G	NP_059989.2:p.Pro1413Ala
NM_020732.3:c.4276C>G	NP_065783.3:p.Pro1426Ala
XM_005267069.3:c.4396C>G	XP_005267126.2:p.Pro1466Ala
XM_011535984.1:c.3475C>G	XP_011534286.1:p.Pro1159Ala
XM_011535985.1:c.3295C>G	XP_011534287.1:p.Pro1099Ala
XM_011535986.1:c.3055C>G	XP_011534288.1:p.Pro1019Ala
XM_011535987.1:c.2674C>G	XP_011534289.1:p.Pro892Ala
XM_011535988.1:c.1537C>G	XP_011534290.1:p.Pro513Ala
NM_001346813.1:c.4396C>G	NP_001333742.1:p.Pro1466Ala
NM_001363725.1:c.2146C>G	NP_001350654.1:p.Pro716Ala
XM_011535984.2:c.4606C>G	XP_011534286.2:p.Pro1536Ala
XM_011535988.3:c.1537C>G	XP_011534290.1:p.Pro513Ala
XM_017011103.2:c.4507C>G	XP_016866592.1:p.Pro1503Ala
XM_017011104.1:c.4477C>G	XP_016866593.1:p.Pro1493Ala
XM_017011105.2:c.4447C>G	XP_016866594.1:p.Pro1483Ala
XM_017011106.2:c.4318C>G	XP_016866595.1:p.Pro1440Ala
XM_017011107.2:c.4297C>G	XP_016866596.1:p.Pro1433Ala
XR_002956289.1:n.4592C>G
NM_001363725.2:c.2146C>G	NP_001350654.1:p.Pro716Ala
NM_001371656.1:c.4525C>G	NP_001358585.1:p.Pro1509Ala
NM_001374820.1:c.4525C>G	NP_001361749.1:p.Pro1509Ala
NM_001374828.1:c.4645C>G MANE Select	NP_001361757.1:p.Pro1549Ala
NM_017519.3:c.4486C>G	NP_059989.3:p.Pro1496Ala