Canonical Allele Identifier: CA452978406

Gene: ARID1B

Linked Data

• dbSNP Id: rs138412834
• COSMIC: COSM5607859 ; COSM5607860
• MyVariant Identifiers: chr6:g.157522192C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201058C>T , CM000668.2:g.157201058C>T	GRCh38
NC_000006.11:g.157522192C>T , CM000668.1:g.157522192C>T	GRCh37
NC_000006.10:g.157563884C>T	NCBI36
NG_032093.1:g.428129C>T
NG_032093.2:g.428129C>T
NG_066624.1:g.430033C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4674C>T	ENSP00000055163.8:p.Pro1558=
ENST00000414678.8:c.4743C>T	ENSP00000412835.3:p.Pro1581=
ENST00000637015.2:c.4962C>T	ENSP00000489729.2:p.Pro1654=
ENST00000346085.10:c.4713C>T	ENSP00000344546.5:p.Pro1571=
ENST00000350026.10:c.4425C>T	ENSP00000055163.7:p.Pro1475=
ENST00000414678.7:c.2991C>T	ENSP00000412835.2:p.Pro997=
ENST00000635849.1:c.2154C>T	ENSP00000490948.1:p.Pro718=
ENST00000635957.1:c.1785C>T	ENSP00000490385.1:p.Pro595=
ENST00000636227.1:n.3296C>T
ENST00000636254.1:n.753C>T
ENST00000636930.2:c.4833C>T MANE Select	ENSP00000490491.2:p.Pro1611=
ENST00000636940.1:n.2830C>T
ENST00000637015.1:c.2201C>T
ENST00000637568.1:c.2115C>T
ENST00000637741.1:n.1499C>T
ENST00000637810.1:c.2175C>T	ENSP00000489636.1:p.Pro725=
ENST00000637904.1:c.2334C>T	ENSP00000490550.1:p.Pro778=
ENST00000647938.1:c.4464C>T	ENSP00000498155.1:p.Pro1488=
ENST00000346085.9:c.4464C>T	ENSP00000344546.4:p.Pro1488=
ENST00000350026.9:c.4425C>T	ENSP00000055163.7:p.Pro1475=
ENST00000414678.6:c.2991C>T	ENSP00000412835.2:p.Pro997=
NM_017519.2:c.4425C>T	NP_059989.2:p.Pro1475=
NM_020732.3:c.4464C>T	NP_065783.3:p.Pro1488=
XM_005267069.3:c.4584C>T	XP_005267126.2:p.Pro1528=
XM_011535984.1:c.3663C>T	XP_011534286.1:p.Pro1221=
XM_011535985.1:c.3483C>T	XP_011534287.1:p.Pro1161=
XM_011535986.1:c.3243C>T	XP_011534288.1:p.Pro1081=
XM_011535987.1:c.2862C>T	XP_011534289.1:p.Pro954=
XM_011535988.1:c.1725C>T	XP_011534290.1:p.Pro575=
NM_001346813.1:c.4584C>T	NP_001333742.1:p.Pro1528=
NM_001363725.1:c.2334C>T	NP_001350654.1:p.Pro778=
XM_011535984.2:c.4794C>T	XP_011534286.2:p.Pro1598=
XM_011535988.3:c.1725C>T	XP_011534290.1:p.Pro575=
XM_017011103.2:c.4695C>T	XP_016866592.1:p.Pro1565=
XM_017011104.1:c.4665C>T	XP_016866593.1:p.Pro1555=
XM_017011105.2:c.4635C>T	XP_016866594.1:p.Pro1545=
XM_017011106.2:c.4506C>T	XP_016866595.1:p.Pro1502=
XM_017011107.2:c.4485C>T	XP_016866596.1:p.Pro1495=
XR_002956289.1:n.4780C>T
NM_001363725.2:c.2334C>T	NP_001350654.1:p.Pro778=
NM_001371656.1:c.4713C>T	NP_001358585.1:p.Pro1571=
NM_001374820.1:c.4713C>T	NP_001361749.1:p.Pro1571=
NM_001374828.1:c.4833C>T MANE Select	NP_001361757.1:p.Pro1611=
NM_017519.3:c.4674C>T	NP_059989.3:p.Pro1558=