Canonical Allele Identifier: CA366234877

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511197C>G (hg19) ; chr6:g.157190063C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190063C>G , CM000668.2:g.157190063C>G	GRCh38
NC_000006.11:g.157511197C>G , CM000668.1:g.157511197C>G	GRCh37
NC_000006.10:g.157552889C>G	NCBI36
NG_032093.1:g.417134C>G
NG_032093.2:g.417134C>G
NG_066624.1:g.419038C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3925C>G	ENSP00000055163.8:p.Pro1309Ala
ENST00000414678.8:c.3994C>G	ENSP00000412835.3:p.Pro1332Ala
ENST00000637015.2:c.4213C>G	ENSP00000489729.2:p.Pro1405Ala
ENST00000346085.10:c.3964C>G	ENSP00000344546.5:p.Pro1322Ala
ENST00000350026.10:c.3676C>G	ENSP00000055163.7:p.Pro1226Ala
ENST00000414678.7:c.2242C>G	ENSP00000412835.2:p.Pro748Ala
ENST00000635849.1:c.1405C>G	ENSP00000490948.1:p.Pro469Ala
ENST00000635957.1:c.1036C>G	ENSP00000490385.1:p.Pro346Ala
ENST00000636930.2:c.4084C>G MANE Select	ENSP00000490491.2:p.Pro1362Ala
ENST00000636940.1:n.2081C>G
ENST00000637015.1:c.1452C>G
ENST00000637568.1:c.1366C>G
ENST00000637741.1:n.750C>G
ENST00000637810.1:c.1426C>G	ENSP00000489636.1:p.Pro476Ala
ENST00000637904.1:c.1585C>G	ENSP00000490550.1:p.Pro529Ala
ENST00000647938.1:c.3715C>G	ENSP00000498155.1:p.Pro1239Ala
ENST00000346085.9:c.3715C>G	ENSP00000344546.4:p.Pro1239Ala
ENST00000350026.9:c.3676C>G	ENSP00000055163.7:p.Pro1226Ala
ENST00000414678.6:c.2242C>G	ENSP00000412835.2:p.Pro748Ala
NM_017519.2:c.3676C>G	NP_059989.2:p.Pro1226Ala
NM_020732.3:c.3715C>G	NP_065783.3:p.Pro1239Ala
XM_005267069.3:c.3835C>G	XP_005267126.2:p.Pro1279Ala
XM_011535984.1:c.2914C>G	XP_011534286.1:p.Pro972Ala
XM_011535985.1:c.2734C>G	XP_011534287.1:p.Pro912Ala
XM_011535986.1:c.2494C>G	XP_011534288.1:p.Pro832Ala
XM_011535987.1:c.2113C>G	XP_011534289.1:p.Pro705Ala
XM_011535988.1:c.976C>G	XP_011534290.1:p.Pro326Ala
NM_001346813.1:c.3835C>G	NP_001333742.1:p.Pro1279Ala
NM_001363725.1:c.1585C>G	NP_001350654.1:p.Pro529Ala
XM_011535984.2:c.4045C>G	XP_011534286.2:p.Pro1349Ala
XM_011535988.3:c.976C>G	XP_011534290.1:p.Pro326Ala
XM_017011103.2:c.3946C>G	XP_016866592.1:p.Pro1316Ala
XM_017011104.1:c.3916C>G	XP_016866593.1:p.Pro1306Ala
XM_017011105.2:c.3886C>G	XP_016866594.1:p.Pro1296Ala
XM_017011106.2:c.3757C>G	XP_016866595.1:p.Pro1253Ala
XM_017011107.2:c.3736C>G	XP_016866596.1:p.Pro1246Ala
XR_002956289.1:n.4128C>G
NM_001363725.2:c.1585C>G	NP_001350654.1:p.Pro529Ala
NM_001371656.1:c.3964C>G	NP_001358585.1:p.Pro1322Ala
NM_001374820.1:c.3964C>G	NP_001361749.1:p.Pro1322Ala
NM_001374828.1:c.4084C>G MANE Select	NP_001361757.1:p.Pro1362Ala
NM_017519.3:c.3925C>G	NP_059989.3:p.Pro1309Ala