Canonical Allele Identifier: CA366227403

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128316940
• COSMIC: COSM5869646 ; COSM5869647
• MyVariant Identifiers: chr6:g.157502166C>T (hg19) ; chr6:g.157181032C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181032C>T , CM000668.2:g.157181032C>T	GRCh38
NC_000006.11:g.157502166C>T , CM000668.1:g.157502166C>T	GRCh37
NC_000006.10:g.157543858C>T	NCBI36
NG_032093.1:g.408103C>T
NG_032093.2:g.408103C>T
NG_066624.1:g.410007C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3409C>T	ENSP00000055163.8:p.Pro1137Ser
ENST00000414678.8:c.3478C>T	ENSP00000412835.3:p.Pro1160Ser
ENST00000637015.2:c.3697C>T	ENSP00000489729.2:p.Pro1233Ser
ENST00000319584.11:c.1582C>T	ENSP00000313006.7:p.Pro528Ser
ENST00000346085.10:c.3448C>T	ENSP00000344546.5:p.Pro1150Ser
ENST00000350026.10:c.3160C>T	ENSP00000055163.7:p.Pro1054Ser
ENST00000414678.7:c.1726C>T	ENSP00000412835.2:p.Pro576Ser
ENST00000635849.1:c.889C>T	ENSP00000490948.1:p.Pro297Ser
ENST00000635957.1:c.523C>T	ENSP00000490385.1:p.Pro175Ser
ENST00000636930.2:c.3568C>T MANE Select	ENSP00000490491.2:p.Pro1190Ser
ENST00000636940.1:n.1565C>T
ENST00000637015.1:c.936C>T
ENST00000637568.1:c.850C>T
ENST00000637741.1:n.234C>T
ENST00000637810.1:c.910C>T	ENSP00000489636.1:p.Pro304Ser
ENST00000637904.1:c.1069C>T	ENSP00000490550.1:p.Pro357Ser
ENST00000647938.1:c.3199C>T	ENSP00000498155.1:p.Pro1067Ser
ENST00000319584.10:c.1585C>T	ENSP00000313006.6:p.Pro529Ser
ENST00000346085.9:c.3199C>T	ENSP00000344546.4:p.Pro1067Ser
ENST00000350026.9:c.3160C>T	ENSP00000055163.7:p.Pro1054Ser
ENST00000400790.3:c.361C>T	ENSP00000383596.3:p.Pro121Ser
ENST00000414678.6:c.1726C>T	ENSP00000412835.2:p.Pro576Ser
ENST00000478761.3:c.770C>T
NM_017519.2:c.3160C>T	NP_059989.2:p.Pro1054Ser
NM_020732.3:c.3199C>T	NP_065783.3:p.Pro1067Ser
XM_005267069.3:c.3319C>T	XP_005267126.2:p.Pro1107Ser
XM_011535984.1:c.2398C>T	XP_011534286.1:p.Pro800Ser
XM_011535985.1:c.2218C>T	XP_011534287.1:p.Pro740Ser
XM_011535986.1:c.1978C>T	XP_011534288.1:p.Pro660Ser
XM_011535987.1:c.1597C>T	XP_011534289.1:p.Pro533Ser
XM_011535988.1:c.460C>T	XP_011534290.1:p.Pro154Ser
NM_001346813.1:c.3319C>T	NP_001333742.1:p.Pro1107Ser
NM_001363725.1:c.1069C>T	NP_001350654.1:p.Pro357Ser
XM_011535984.2:c.3529C>T	XP_011534286.2:p.Pro1177Ser
XM_011535988.3:c.460C>T	XP_011534290.1:p.Pro154Ser
XM_017011103.2:c.3430C>T	XP_016866592.1:p.Pro1144Ser
XM_017011104.1:c.3400C>T	XP_016866593.1:p.Pro1134Ser
XM_017011105.2:c.3370C>T	XP_016866594.1:p.Pro1124Ser
XM_017011106.2:c.3241C>T	XP_016866595.1:p.Pro1081Ser
XM_017011107.2:c.3220C>T	XP_016866596.1:p.Pro1074Ser
XR_002956289.1:n.3612C>T
NM_001363725.2:c.1069C>T	NP_001350654.1:p.Pro357Ser
NM_001371656.1:c.3448C>T	NP_001358585.1:p.Pro1150Ser
NM_001374820.1:c.3448C>T	NP_001361749.1:p.Pro1150Ser
NM_001374828.1:c.3568C>T MANE Select	NP_001361757.1:p.Pro1190Ser
NM_017519.3:c.3409C>T	NP_059989.3:p.Pro1137Ser