Canonical Allele Identifier: CA366242303

Gene: ARID1B

Linked Data

• COSMIC: COSM4918906 ; COSM4918907
• MyVariant Identifiers: chr6:g.157522371A>G (hg19) ; chr6:g.157201237A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201237A>G , CM000668.2:g.157201237A>G	GRCh38
NC_000006.11:g.157522371A>G , CM000668.1:g.157522371A>G	GRCh37
NC_000006.10:g.157564063A>G	NCBI36
NG_032093.1:g.428308A>G
NG_032093.2:g.428308A>G
NG_066624.1:g.430212A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4853A>G	ENSP00000055163.8:p.Asn1618Ser
ENST00000414678.8:c.4922A>G	ENSP00000412835.3:p.Asn1641Ser
ENST00000637015.2:c.5141A>G	ENSP00000489729.2:p.Asn1714Ser
ENST00000346085.10:c.4892A>G	ENSP00000344546.5:p.Asn1631Ser
ENST00000350026.10:c.4604A>G	ENSP00000055163.7:p.Asn1535Ser
ENST00000414678.7:c.3170A>G	ENSP00000412835.2:p.Asn1057Ser
ENST00000635849.1:c.2333A>G	ENSP00000490948.1:p.Asn778Ser
ENST00000635957.1:c.1964A>G	ENSP00000490385.1:p.Asn655Ser
ENST00000636227.1:n.3475A>G
ENST00000636254.1:n.932A>G
ENST00000636930.2:c.5012A>G MANE Select	ENSP00000490491.2:p.Asn1671Ser
ENST00000636940.1:n.3009A>G
ENST00000637015.1:c.2380A>G
ENST00000637568.1:c.2294A>G
ENST00000637741.1:n.1678A>G
ENST00000637810.1:c.2354A>G	ENSP00000489636.1:p.Asn785Ser
ENST00000637904.1:c.2513A>G	ENSP00000490550.1:p.Asn838Ser
ENST00000647938.1:c.4643A>G	ENSP00000498155.1:p.Asn1548Ser
ENST00000346085.9:c.4643A>G	ENSP00000344546.4:p.Asn1548Ser
ENST00000350026.9:c.4604A>G	ENSP00000055163.7:p.Asn1535Ser
ENST00000414678.6:c.3170A>G	ENSP00000412835.2:p.Asn1057Ser
NM_017519.2:c.4604A>G	NP_059989.2:p.Asn1535Ser
NM_020732.3:c.4643A>G	NP_065783.3:p.Asn1548Ser
XM_005267069.3:c.4763A>G	XP_005267126.2:p.Asn1588Ser
XM_011535984.1:c.3842A>G	XP_011534286.1:p.Asn1281Ser
XM_011535985.1:c.3662A>G	XP_011534287.1:p.Asn1221Ser
XM_011535986.1:c.3422A>G	XP_011534288.1:p.Asn1141Ser
XM_011535987.1:c.3041A>G	XP_011534289.1:p.Asn1014Ser
XM_011535988.1:c.1904A>G	XP_011534290.1:p.Asn635Ser
NM_001346813.1:c.4763A>G	NP_001333742.1:p.Asn1588Ser
NM_001363725.1:c.2513A>G	NP_001350654.1:p.Asn838Ser
XM_011535984.2:c.4973A>G	XP_011534286.2:p.Asn1658Ser
XM_011535988.3:c.1904A>G	XP_011534290.1:p.Asn635Ser
XM_017011103.2:c.4874A>G	XP_016866592.1:p.Asn1625Ser
XM_017011104.1:c.4844A>G	XP_016866593.1:p.Asn1615Ser
XM_017011105.2:c.4814A>G	XP_016866594.1:p.Asn1605Ser
XM_017011106.2:c.4685A>G	XP_016866595.1:p.Asn1562Ser
XM_017011107.2:c.4664A>G	XP_016866596.1:p.Asn1555Ser
XR_002956289.1:n.4959A>G
NM_001363725.2:c.2513A>G	NP_001350654.1:p.Asn838Ser
NM_001371656.1:c.4892A>G	NP_001358585.1:p.Asn1631Ser
NM_001374820.1:c.4892A>G	NP_001361749.1:p.Asn1631Ser
NM_001374828.1:c.5012A>G MANE Select	NP_001361757.1:p.Asn1671Ser
NM_017519.3:c.4853A>G	NP_059989.3:p.Asn1618Ser