Canonical Allele Identifier: CA366241755

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522193C>G (hg19) ; chr6:g.157201059C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201059C>G , CM000668.2:g.157201059C>G	GRCh38
NC_000006.11:g.157522193C>G , CM000668.1:g.157522193C>G	GRCh37
NC_000006.10:g.157563885C>G	NCBI36
NG_032093.1:g.428130C>G
NG_032093.2:g.428130C>G
NG_066624.1:g.430034C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4675C>G	ENSP00000055163.8:p.Pro1559Ala
ENST00000414678.8:c.4744C>G	ENSP00000412835.3:p.Pro1582Ala
ENST00000637015.2:c.4963C>G	ENSP00000489729.2:p.Pro1655Ala
ENST00000346085.10:c.4714C>G	ENSP00000344546.5:p.Pro1572Ala
ENST00000350026.10:c.4426C>G	ENSP00000055163.7:p.Pro1476Ala
ENST00000414678.7:c.2992C>G	ENSP00000412835.2:p.Pro998Ala
ENST00000635849.1:c.2155C>G	ENSP00000490948.1:p.Pro719Ala
ENST00000635957.1:c.1786C>G	ENSP00000490385.1:p.Pro596Ala
ENST00000636227.1:n.3297C>G
ENST00000636254.1:n.754C>G
ENST00000636930.2:c.4834C>G MANE Select	ENSP00000490491.2:p.Pro1612Ala
ENST00000636940.1:n.2831C>G
ENST00000637015.1:c.2202C>G
ENST00000637568.1:c.2116C>G
ENST00000637741.1:n.1500C>G
ENST00000637810.1:c.2176C>G	ENSP00000489636.1:p.Pro726Ala
ENST00000637904.1:c.2335C>G	ENSP00000490550.1:p.Pro779Ala
ENST00000647938.1:c.4465C>G	ENSP00000498155.1:p.Pro1489Ala
ENST00000346085.9:c.4465C>G	ENSP00000344546.4:p.Pro1489Ala
ENST00000350026.9:c.4426C>G	ENSP00000055163.7:p.Pro1476Ala
ENST00000414678.6:c.2992C>G	ENSP00000412835.2:p.Pro998Ala
NM_017519.2:c.4426C>G	NP_059989.2:p.Pro1476Ala
NM_020732.3:c.4465C>G	NP_065783.3:p.Pro1489Ala
XM_005267069.3:c.4585C>G	XP_005267126.2:p.Pro1529Ala
XM_011535984.1:c.3664C>G	XP_011534286.1:p.Pro1222Ala
XM_011535985.1:c.3484C>G	XP_011534287.1:p.Pro1162Ala
XM_011535986.1:c.3244C>G	XP_011534288.1:p.Pro1082Ala
XM_011535987.1:c.2863C>G	XP_011534289.1:p.Pro955Ala
XM_011535988.1:c.1726C>G	XP_011534290.1:p.Pro576Ala
NM_001346813.1:c.4585C>G	NP_001333742.1:p.Pro1529Ala
NM_001363725.1:c.2335C>G	NP_001350654.1:p.Pro779Ala
XM_011535984.2:c.4795C>G	XP_011534286.2:p.Pro1599Ala
XM_011535988.3:c.1726C>G	XP_011534290.1:p.Pro576Ala
XM_017011103.2:c.4696C>G	XP_016866592.1:p.Pro1566Ala
XM_017011104.1:c.4666C>G	XP_016866593.1:p.Pro1556Ala
XM_017011105.2:c.4636C>G	XP_016866594.1:p.Pro1546Ala
XM_017011106.2:c.4507C>G	XP_016866595.1:p.Pro1503Ala
XM_017011107.2:c.4486C>G	XP_016866596.1:p.Pro1496Ala
XR_002956289.1:n.4781C>G
NM_001363725.2:c.2335C>G	NP_001350654.1:p.Pro779Ala
NM_001371656.1:c.4714C>G	NP_001358585.1:p.Pro1572Ala
NM_001374820.1:c.4714C>G	NP_001361749.1:p.Pro1572Ala
NM_001374828.1:c.4834C>G MANE Select	NP_001361757.1:p.Pro1612Ala
NM_017519.3:c.4675C>G	NP_059989.3:p.Pro1559Ala