Canonical Allele Identifier: CA452784792

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522513A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201379A>G , CM000668.2:g.157201379A>G	GRCh38
NC_000006.11:g.157522513A>G , CM000668.1:g.157522513A>G	GRCh37
NC_000006.10:g.157564205A>G	NCBI36
NG_032093.1:g.428450A>G
NG_032093.2:g.428450A>G
NG_066624.1:g.430354A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4995A>G	ENSP00000055163.8:p.Pro1665=
ENST00000414678.8:c.5064A>G	ENSP00000412835.3:p.Pro1688=
ENST00000637015.2:c.5283A>G	ENSP00000489729.2:p.Pro1761=
ENST00000346085.10:c.5034A>G	ENSP00000344546.5:p.Pro1678=
ENST00000350026.10:c.4746A>G	ENSP00000055163.7:p.Pro1582=
ENST00000414678.7:c.3312A>G	ENSP00000412835.2:p.Pro1104=
ENST00000635849.1:c.2475A>G	ENSP00000490948.1:p.Pro825=
ENST00000635957.1:c.2106A>G	ENSP00000490385.1:p.Pro702=
ENST00000636227.1:n.3617A>G
ENST00000636254.1:n.1074A>G
ENST00000636930.2:c.5154A>G MANE Select	ENSP00000490491.2:p.Pro1718=
ENST00000636940.1:n.3151A>G
ENST00000637015.1:c.2522A>G
ENST00000637568.1:c.2436A>G
ENST00000637741.1:n.1820A>G
ENST00000637810.1:c.2496A>G	ENSP00000489636.1:p.Pro832=
ENST00000637904.1:c.2655A>G	ENSP00000490550.1:p.Pro885=
ENST00000647938.1:c.4785A>G	ENSP00000498155.1:p.Pro1595=
ENST00000346085.9:c.4785A>G	ENSP00000344546.4:p.Pro1595=
ENST00000350026.9:c.4746A>G	ENSP00000055163.7:p.Pro1582=
ENST00000414678.6:c.3312A>G	ENSP00000412835.2:p.Pro1104=
NM_017519.2:c.4746A>G	NP_059989.2:p.Pro1582=
NM_020732.3:c.4785A>G	NP_065783.3:p.Pro1595=
XM_005267069.3:c.4905A>G	XP_005267126.2:p.Pro1635=
XM_011535984.1:c.3984A>G	XP_011534286.1:p.Pro1328=
XM_011535985.1:c.3804A>G	XP_011534287.1:p.Pro1268=
XM_011535986.1:c.3564A>G	XP_011534288.1:p.Pro1188=
XM_011535987.1:c.3183A>G	XP_011534289.1:p.Pro1061=
XM_011535988.1:c.2046A>G	XP_011534290.1:p.Pro682=
NM_001346813.1:c.4905A>G	NP_001333742.1:p.Pro1635=
NM_001363725.1:c.2655A>G	NP_001350654.1:p.Pro885=
XM_011535984.2:c.5115A>G	XP_011534286.2:p.Pro1705=
XM_011535988.3:c.2046A>G	XP_011534290.1:p.Pro682=
XM_017011103.2:c.5016A>G	XP_016866592.1:p.Pro1672=
XM_017011104.1:c.4986A>G	XP_016866593.1:p.Pro1662=
XM_017011105.2:c.4956A>G	XP_016866594.1:p.Pro1652=
XM_017011106.2:c.4827A>G	XP_016866595.1:p.Pro1609=
XM_017011107.2:c.4806A>G	XP_016866596.1:p.Pro1602=
XR_002956289.1:n.5101A>G
NM_001363725.2:c.2655A>G	NP_001350654.1:p.Pro885=
NM_001371656.1:c.5034A>G	NP_001358585.1:p.Pro1678=
NM_001374820.1:c.5034A>G	NP_001361749.1:p.Pro1678=
NM_001374828.1:c.5154A>G MANE Select	NP_001361757.1:p.Pro1718=
NM_017519.3:c.4995A>G	NP_059989.3:p.Pro1665=