Canonical Allele Identifier: CA366241353

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522112C>A (hg19) ; chr6:g.157200978C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200978C>A , CM000668.2:g.157200978C>A	GRCh38
NC_000006.11:g.157522112C>A , CM000668.1:g.157522112C>A	GRCh37
NC_000006.10:g.157563804C>A	NCBI36
NG_032093.1:g.428049C>A
NG_032093.2:g.428049C>A
NG_066624.1:g.429953C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4594C>A	ENSP00000055163.8:p.Gln1532Lys
ENST00000414678.8:c.4663C>A	ENSP00000412835.3:p.Gln1555Lys
ENST00000637015.2:c.4882C>A	ENSP00000489729.2:p.Gln1628Lys
ENST00000346085.10:c.4633C>A	ENSP00000344546.5:p.Gln1545Lys
ENST00000350026.10:c.4345C>A	ENSP00000055163.7:p.Gln1449Lys
ENST00000414678.7:c.2911C>A	ENSP00000412835.2:p.Gln971Lys
ENST00000635849.1:c.2074C>A	ENSP00000490948.1:p.Gln692Lys
ENST00000635957.1:c.1705C>A	ENSP00000490385.1:p.Gln569Lys
ENST00000636227.1:n.3216C>A
ENST00000636254.1:n.673C>A
ENST00000636930.2:c.4753C>A MANE Select	ENSP00000490491.2:p.Gln1585Lys
ENST00000636940.1:n.2750C>A
ENST00000637015.1:c.2121C>A
ENST00000637568.1:c.2035C>A
ENST00000637741.1:n.1419C>A
ENST00000637810.1:c.2095C>A	ENSP00000489636.1:p.Gln699Lys
ENST00000637904.1:c.2254C>A	ENSP00000490550.1:p.Gln752Lys
ENST00000647938.1:c.4384C>A	ENSP00000498155.1:p.Gln1462Lys
ENST00000346085.9:c.4384C>A	ENSP00000344546.4:p.Gln1462Lys
ENST00000350026.9:c.4345C>A	ENSP00000055163.7:p.Gln1449Lys
ENST00000414678.6:c.2911C>A	ENSP00000412835.2:p.Gln971Lys
NM_017519.2:c.4345C>A	NP_059989.2:p.Gln1449Lys
NM_020732.3:c.4384C>A	NP_065783.3:p.Gln1462Lys
XM_005267069.3:c.4504C>A	XP_005267126.2:p.Gln1502Lys
XM_011535984.1:c.3583C>A	XP_011534286.1:p.Gln1195Lys
XM_011535985.1:c.3403C>A	XP_011534287.1:p.Gln1135Lys
XM_011535986.1:c.3163C>A	XP_011534288.1:p.Gln1055Lys
XM_011535987.1:c.2782C>A	XP_011534289.1:p.Gln928Lys
XM_011535988.1:c.1645C>A	XP_011534290.1:p.Gln549Lys
NM_001346813.1:c.4504C>A	NP_001333742.1:p.Gln1502Lys
NM_001363725.1:c.2254C>A	NP_001350654.1:p.Gln752Lys
XM_011535984.2:c.4714C>A	XP_011534286.2:p.Gln1572Lys
XM_011535988.3:c.1645C>A	XP_011534290.1:p.Gln549Lys
XM_017011103.2:c.4615C>A	XP_016866592.1:p.Gln1539Lys
XM_017011104.1:c.4585C>A	XP_016866593.1:p.Gln1529Lys
XM_017011105.2:c.4555C>A	XP_016866594.1:p.Gln1519Lys
XM_017011106.2:c.4426C>A	XP_016866595.1:p.Gln1476Lys
XM_017011107.2:c.4405C>A	XP_016866596.1:p.Gln1469Lys
XR_002956289.1:n.4700C>A
NM_001363725.2:c.2254C>A	NP_001350654.1:p.Gln752Lys
NM_001371656.1:c.4633C>A	NP_001358585.1:p.Gln1545Lys
NM_001374820.1:c.4633C>A	NP_001361749.1:p.Gln1545Lys
NM_001374828.1:c.4753C>A MANE Select	NP_001361757.1:p.Gln1585Lys
NM_017519.3:c.4594C>A	NP_059989.3:p.Gln1532Lys