Canonical Allele Identifier: CA366239696

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157519983C>A (hg19) ; chr6:g.157198849C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198849C>A , CM000668.2:g.157198849C>A	GRCh38
NC_000006.11:g.157519983C>A , CM000668.1:g.157519983C>A	GRCh37
NC_000006.10:g.157561675C>A	NCBI36
NG_032093.1:g.425920C>A
NG_032093.2:g.425920C>A
NG_066624.1:g.427824C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4262C>A	ENSP00000055163.8:p.Pro1421His
ENST00000414678.8:c.4331C>A	ENSP00000412835.3:p.Pro1444His
ENST00000637015.2:c.4550C>A	ENSP00000489729.2:p.Pro1517His
ENST00000346085.10:c.4301C>A	ENSP00000344546.5:p.Pro1434His
ENST00000350026.10:c.4013C>A	ENSP00000055163.7:p.Pro1338His
ENST00000414678.7:c.2579C>A	ENSP00000412835.2:p.Pro860His
ENST00000635849.1:c.1742C>A	ENSP00000490948.1:p.Pro581His
ENST00000635957.1:c.1373C>A	ENSP00000490385.1:p.Pro458His
ENST00000636227.1:n.2884C>A
ENST00000636254.1:n.341C>A
ENST00000636930.2:c.4421C>A MANE Select	ENSP00000490491.2:p.Pro1474His
ENST00000636940.1:n.2418C>A
ENST00000637015.1:c.1789C>A
ENST00000637568.1:c.1703C>A
ENST00000637741.1:n.1087C>A
ENST00000637810.1:c.1763C>A	ENSP00000489636.1:p.Pro588His
ENST00000637904.1:c.1922C>A	ENSP00000490550.1:p.Pro641His
ENST00000647938.1:c.4052C>A	ENSP00000498155.1:p.Pro1351His
ENST00000346085.9:c.4052C>A	ENSP00000344546.4:p.Pro1351His
ENST00000350026.9:c.4013C>A	ENSP00000055163.7:p.Pro1338His
ENST00000414678.6:c.2579C>A	ENSP00000412835.2:p.Pro860His
NM_017519.2:c.4013C>A	NP_059989.2:p.Pro1338His
NM_020732.3:c.4052C>A	NP_065783.3:p.Pro1351His
XM_005267069.3:c.4172C>A	XP_005267126.2:p.Pro1391His
XM_011535984.1:c.3251C>A	XP_011534286.1:p.Pro1084His
XM_011535985.1:c.3071C>A	XP_011534287.1:p.Pro1024His
XM_011535986.1:c.2831C>A	XP_011534288.1:p.Pro944His
XM_011535987.1:c.2450C>A	XP_011534289.1:p.Pro817His
XM_011535988.1:c.1313C>A	XP_011534290.1:p.Pro438His
NM_001346813.1:c.4172C>A	NP_001333742.1:p.Pro1391His
NM_001363725.1:c.1922C>A	NP_001350654.1:p.Pro641His
XM_011535984.2:c.4382C>A	XP_011534286.2:p.Pro1461His
XM_011535988.3:c.1313C>A	XP_011534290.1:p.Pro438His
XM_017011103.2:c.4283C>A	XP_016866592.1:p.Pro1428His
XM_017011104.1:c.4253C>A	XP_016866593.1:p.Pro1418His
XM_017011105.2:c.4223C>A	XP_016866594.1:p.Pro1408His
XM_017011106.2:c.4094C>A	XP_016866595.1:p.Pro1365His
XM_017011107.2:c.4073C>A	XP_016866596.1:p.Pro1358His
XR_002956289.1:n.4427-1856C>A
NM_001363725.2:c.1922C>A	NP_001350654.1:p.Pro641His
NM_001371656.1:c.4301C>A	NP_001358585.1:p.Pro1434His
NM_001374820.1:c.4301C>A	NP_001361749.1:p.Pro1434His
NM_001374828.1:c.4421C>A MANE Select	NP_001361757.1:p.Pro1474His
NM_017519.3:c.4262C>A	NP_059989.3:p.Pro1421His