Canonical Allele Identifier: CA366239686

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366173
• MyVariant Identifiers: chr6:g.157519982C>A (hg19) ; chr6:g.157198848C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198848C>A , CM000668.2:g.157198848C>A	GRCh38
NC_000006.11:g.157519982C>A , CM000668.1:g.157519982C>A	GRCh37
NC_000006.10:g.157561674C>A	NCBI36
NG_032093.1:g.425919C>A
NG_032093.2:g.425919C>A
NG_066624.1:g.427823C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4261C>A	ENSP00000055163.8:p.Pro1421Thr
ENST00000414678.8:c.4330C>A	ENSP00000412835.3:p.Pro1444Thr
ENST00000637015.2:c.4549C>A	ENSP00000489729.2:p.Pro1517Thr
ENST00000346085.10:c.4300C>A	ENSP00000344546.5:p.Pro1434Thr
ENST00000350026.10:c.4012C>A	ENSP00000055163.7:p.Pro1338Thr
ENST00000414678.7:c.2578C>A	ENSP00000412835.2:p.Pro860Thr
ENST00000635849.1:c.1741C>A	ENSP00000490948.1:p.Pro581Thr
ENST00000635957.1:c.1372C>A	ENSP00000490385.1:p.Pro458Thr
ENST00000636227.1:n.2883C>A
ENST00000636254.1:n.340C>A
ENST00000636930.2:c.4420C>A MANE Select	ENSP00000490491.2:p.Pro1474Thr
ENST00000636940.1:n.2417C>A
ENST00000637015.1:c.1788C>A
ENST00000637568.1:c.1702C>A
ENST00000637741.1:n.1086C>A
ENST00000637810.1:c.1762C>A	ENSP00000489636.1:p.Pro588Thr
ENST00000637904.1:c.1921C>A	ENSP00000490550.1:p.Pro641Thr
ENST00000647938.1:c.4051C>A	ENSP00000498155.1:p.Pro1351Thr
ENST00000346085.9:c.4051C>A	ENSP00000344546.4:p.Pro1351Thr
ENST00000350026.9:c.4012C>A	ENSP00000055163.7:p.Pro1338Thr
ENST00000414678.6:c.2578C>A	ENSP00000412835.2:p.Pro860Thr
NM_017519.2:c.4012C>A	NP_059989.2:p.Pro1338Thr
NM_020732.3:c.4051C>A	NP_065783.3:p.Pro1351Thr
XM_005267069.3:c.4171C>A	XP_005267126.2:p.Pro1391Thr
XM_011535984.1:c.3250C>A	XP_011534286.1:p.Pro1084Thr
XM_011535985.1:c.3070C>A	XP_011534287.1:p.Pro1024Thr
XM_011535986.1:c.2830C>A	XP_011534288.1:p.Pro944Thr
XM_011535987.1:c.2449C>A	XP_011534289.1:p.Pro817Thr
XM_011535988.1:c.1312C>A	XP_011534290.1:p.Pro438Thr
NM_001346813.1:c.4171C>A	NP_001333742.1:p.Pro1391Thr
NM_001363725.1:c.1921C>A	NP_001350654.1:p.Pro641Thr
XM_011535984.2:c.4381C>A	XP_011534286.2:p.Pro1461Thr
XM_011535988.3:c.1312C>A	XP_011534290.1:p.Pro438Thr
XM_017011103.2:c.4282C>A	XP_016866592.1:p.Pro1428Thr
XM_017011104.1:c.4252C>A	XP_016866593.1:p.Pro1418Thr
XM_017011105.2:c.4222C>A	XP_016866594.1:p.Pro1408Thr
XM_017011106.2:c.4093C>A	XP_016866595.1:p.Pro1365Thr
XM_017011107.2:c.4072C>A	XP_016866596.1:p.Pro1358Thr
XR_002956289.1:n.4427-1857C>A
NM_001363725.2:c.1921C>A	NP_001350654.1:p.Pro641Thr
NM_001371656.1:c.4300C>A	NP_001358585.1:p.Pro1434Thr
NM_001374820.1:c.4300C>A	NP_001361749.1:p.Pro1434Thr
NM_001374828.1:c.4420C>A MANE Select	NP_001361757.1:p.Pro1474Thr
NM_017519.3:c.4261C>A	NP_059989.3:p.Pro1421Thr