Canonical Allele Identifier: CA366242130

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522290C>A (hg19) ; chr6:g.157201156C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201156C>A , CM000668.2:g.157201156C>A	GRCh38
NC_000006.11:g.157522290C>A , CM000668.1:g.157522290C>A	GRCh37
NC_000006.10:g.157563982C>A	NCBI36
NG_032093.1:g.428227C>A
NG_032093.2:g.428227C>A
NG_066624.1:g.430131C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4772C>A	ENSP00000055163.8:p.Pro1591His
ENST00000414678.8:c.4841C>A	ENSP00000412835.3:p.Pro1614His
ENST00000637015.2:c.5060C>A	ENSP00000489729.2:p.Pro1687His
ENST00000346085.10:c.4811C>A	ENSP00000344546.5:p.Pro1604His
ENST00000350026.10:c.4523C>A	ENSP00000055163.7:p.Pro1508His
ENST00000414678.7:c.3089C>A	ENSP00000412835.2:p.Pro1030His
ENST00000635849.1:c.2252C>A	ENSP00000490948.1:p.Pro751His
ENST00000635957.1:c.1883C>A	ENSP00000490385.1:p.Pro628His
ENST00000636227.1:n.3394C>A
ENST00000636254.1:n.851C>A
ENST00000636930.2:c.4931C>A MANE Select	ENSP00000490491.2:p.Pro1644His
ENST00000636940.1:n.2928C>A
ENST00000637015.1:c.2299C>A
ENST00000637568.1:c.2213C>A
ENST00000637741.1:n.1597C>A
ENST00000637810.1:c.2273C>A	ENSP00000489636.1:p.Pro758His
ENST00000637904.1:c.2432C>A	ENSP00000490550.1:p.Pro811His
ENST00000647938.1:c.4562C>A	ENSP00000498155.1:p.Pro1521His
ENST00000346085.9:c.4562C>A	ENSP00000344546.4:p.Pro1521His
ENST00000350026.9:c.4523C>A	ENSP00000055163.7:p.Pro1508His
ENST00000414678.6:c.3089C>A	ENSP00000412835.2:p.Pro1030His
NM_017519.2:c.4523C>A	NP_059989.2:p.Pro1508His
NM_020732.3:c.4562C>A	NP_065783.3:p.Pro1521His
XM_005267069.3:c.4682C>A	XP_005267126.2:p.Pro1561His
XM_011535984.1:c.3761C>A	XP_011534286.1:p.Pro1254His
XM_011535985.1:c.3581C>A	XP_011534287.1:p.Pro1194His
XM_011535986.1:c.3341C>A	XP_011534288.1:p.Pro1114His
XM_011535987.1:c.2960C>A	XP_011534289.1:p.Pro987His
XM_011535988.1:c.1823C>A	XP_011534290.1:p.Pro608His
NM_001346813.1:c.4682C>A	NP_001333742.1:p.Pro1561His
NM_001363725.1:c.2432C>A	NP_001350654.1:p.Pro811His
XM_011535984.2:c.4892C>A	XP_011534286.2:p.Pro1631His
XM_011535988.3:c.1823C>A	XP_011534290.1:p.Pro608His
XM_017011103.2:c.4793C>A	XP_016866592.1:p.Pro1598His
XM_017011104.1:c.4763C>A	XP_016866593.1:p.Pro1588His
XM_017011105.2:c.4733C>A	XP_016866594.1:p.Pro1578His
XM_017011106.2:c.4604C>A	XP_016866595.1:p.Pro1535His
XM_017011107.2:c.4583C>A	XP_016866596.1:p.Pro1528His
XR_002956289.1:n.4878C>A
NM_001363725.2:c.2432C>A	NP_001350654.1:p.Pro811His
NM_001371656.1:c.4811C>A	NP_001358585.1:p.Pro1604His
NM_001374820.1:c.4811C>A	NP_001361749.1:p.Pro1604His
NM_001374828.1:c.4931C>A MANE Select	NP_001361757.1:p.Pro1644His
NM_017519.3:c.4772C>A	NP_059989.3:p.Pro1591His