Canonical Allele Identifier: CA366239692

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157519982C>T (hg19) ; chr6:g.157198848C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4261C>T	ENSP00000055163.8:p.Pro1421Ser
ENST00000414678.8:c.4330C>T	ENSP00000412835.3:p.Pro1444Ser
ENST00000637015.2:c.4549C>T	ENSP00000489729.2:p.Pro1517Ser
ENST00000346085.10:c.4300C>T	ENSP00000344546.5:p.Pro1434Ser
ENST00000350026.10:c.4012C>T	ENSP00000055163.7:p.Pro1338Ser
ENST00000414678.7:c.2578C>T	ENSP00000412835.2:p.Pro860Ser
ENST00000635849.1:c.1741C>T	ENSP00000490948.1:p.Pro581Ser
ENST00000635957.1:c.1372C>T	ENSP00000490385.1:p.Pro458Ser
ENST00000636227.1:n.2883C>T
ENST00000636254.1:n.340C>T
ENST00000636930.2:c.4420C>T MANE Select	ENSP00000490491.2:p.Pro1474Ser
ENST00000636940.1:n.2417C>T
ENST00000637015.1:c.1788C>T
ENST00000637568.1:c.1702C>T
ENST00000637741.1:n.1086C>T
ENST00000637810.1:c.1762C>T	ENSP00000489636.1:p.Pro588Ser
ENST00000637904.1:c.1921C>T	ENSP00000490550.1:p.Pro641Ser
ENST00000647938.1:c.4051C>T	ENSP00000498155.1:p.Pro1351Ser
ENST00000346085.9:c.4051C>T	ENSP00000344546.4:p.Pro1351Ser
ENST00000350026.9:c.4012C>T	ENSP00000055163.7:p.Pro1338Ser
ENST00000414678.6:c.2578C>T	ENSP00000412835.2:p.Pro860Ser
NM_017519.2:c.4012C>T	NP_059989.2:p.Pro1338Ser
NM_020732.3:c.4051C>T	NP_065783.3:p.Pro1351Ser
XM_005267069.3:c.4171C>T	XP_005267126.2:p.Pro1391Ser
XM_011535984.1:c.3250C>T	XP_011534286.1:p.Pro1084Ser
XM_011535985.1:c.3070C>T	XP_011534287.1:p.Pro1024Ser
XM_011535986.1:c.2830C>T	XP_011534288.1:p.Pro944Ser
XM_011535987.1:c.2449C>T	XP_011534289.1:p.Pro817Ser
XM_011535988.1:c.1312C>T	XP_011534290.1:p.Pro438Ser
NM_001346813.1:c.4171C>T	NP_001333742.1:p.Pro1391Ser
NM_001363725.1:c.1921C>T	NP_001350654.1:p.Pro641Ser
XM_011535984.2:c.4381C>T	XP_011534286.2:p.Pro1461Ser
XM_011535988.3:c.1312C>T	XP_011534290.1:p.Pro438Ser
XM_017011103.2:c.4282C>T	XP_016866592.1:p.Pro1428Ser
XM_017011104.1:c.4252C>T	XP_016866593.1:p.Pro1418Ser
XM_017011105.2:c.4222C>T	XP_016866594.1:p.Pro1408Ser
XM_017011106.2:c.4093C>T	XP_016866595.1:p.Pro1365Ser
XM_017011107.2:c.4072C>T	XP_016866596.1:p.Pro1358Ser
XR_002956289.1:n.4427-1857C>T
NM_001363725.2:c.1921C>T	NP_001350654.1:p.Pro641Ser
NM_001371656.1:c.4300C>T	NP_001358585.1:p.Pro1434Ser
NM_001374820.1:c.4300C>T	NP_001361749.1:p.Pro1434Ser
NM_001374828.1:c.4420C>T MANE Select	NP_001361757.1:p.Pro1474Ser
NM_017519.3:c.4261C>T	NP_059989.3:p.Pro1421Ser