Canonical Allele Identifier: CA366227396

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128316940
• MyVariant Identifiers: chr6:g.157502166C>A (hg19) ; chr6:g.157181032C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3409C>A	ENSP00000055163.8:p.Pro1137Thr
ENST00000414678.8:c.3478C>A	ENSP00000412835.3:p.Pro1160Thr
ENST00000637015.2:c.3697C>A	ENSP00000489729.2:p.Pro1233Thr
ENST00000319584.11:c.1582C>A	ENSP00000313006.7:p.Pro528Thr
ENST00000346085.10:c.3448C>A	ENSP00000344546.5:p.Pro1150Thr
ENST00000350026.10:c.3160C>A	ENSP00000055163.7:p.Pro1054Thr
ENST00000414678.7:c.1726C>A	ENSP00000412835.2:p.Pro576Thr
ENST00000635849.1:c.889C>A	ENSP00000490948.1:p.Pro297Thr
ENST00000635957.1:c.523C>A	ENSP00000490385.1:p.Pro175Thr
ENST00000636930.2:c.3568C>A MANE Select	ENSP00000490491.2:p.Pro1190Thr
ENST00000636940.1:n.1565C>A
ENST00000637015.1:c.936C>A
ENST00000637568.1:c.850C>A
ENST00000637741.1:n.234C>A
ENST00000637810.1:c.910C>A	ENSP00000489636.1:p.Pro304Thr
ENST00000637904.1:c.1069C>A	ENSP00000490550.1:p.Pro357Thr
ENST00000647938.1:c.3199C>A	ENSP00000498155.1:p.Pro1067Thr
ENST00000319584.10:c.1585C>A	ENSP00000313006.6:p.Pro529Thr
ENST00000346085.9:c.3199C>A	ENSP00000344546.4:p.Pro1067Thr
ENST00000350026.9:c.3160C>A	ENSP00000055163.7:p.Pro1054Thr
ENST00000400790.3:c.361C>A	ENSP00000383596.3:p.Pro121Thr
ENST00000414678.6:c.1726C>A	ENSP00000412835.2:p.Pro576Thr
ENST00000478761.3:c.770C>A
NM_017519.2:c.3160C>A	NP_059989.2:p.Pro1054Thr
NM_020732.3:c.3199C>A	NP_065783.3:p.Pro1067Thr
XM_005267069.3:c.3319C>A	XP_005267126.2:p.Pro1107Thr
XM_011535984.1:c.2398C>A	XP_011534286.1:p.Pro800Thr
XM_011535985.1:c.2218C>A	XP_011534287.1:p.Pro740Thr
XM_011535986.1:c.1978C>A	XP_011534288.1:p.Pro660Thr
XM_011535987.1:c.1597C>A	XP_011534289.1:p.Pro533Thr
XM_011535988.1:c.460C>A	XP_011534290.1:p.Pro154Thr
NM_001346813.1:c.3319C>A	NP_001333742.1:p.Pro1107Thr
NM_001363725.1:c.1069C>A	NP_001350654.1:p.Pro357Thr
XM_011535984.2:c.3529C>A	XP_011534286.2:p.Pro1177Thr
XM_011535988.3:c.460C>A	XP_011534290.1:p.Pro154Thr
XM_017011103.2:c.3430C>A	XP_016866592.1:p.Pro1144Thr
XM_017011104.1:c.3400C>A	XP_016866593.1:p.Pro1134Thr
XM_017011105.2:c.3370C>A	XP_016866594.1:p.Pro1124Thr
XM_017011106.2:c.3241C>A	XP_016866595.1:p.Pro1081Thr
XM_017011107.2:c.3220C>A	XP_016866596.1:p.Pro1074Thr
XR_002956289.1:n.3612C>A
NM_001363725.2:c.1069C>A	NP_001350654.1:p.Pro357Thr
NM_001371656.1:c.3448C>A	NP_001358585.1:p.Pro1150Thr
NM_001374820.1:c.3448C>A	NP_001361749.1:p.Pro1150Thr
NM_001374828.1:c.3568C>A MANE Select	NP_001361757.1:p.Pro1190Thr
NM_017519.3:c.3409C>A	NP_059989.3:p.Pro1137Thr