Canonical Allele Identifier: CA366241741

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522191C>A (hg19) ; chr6:g.157201057C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201057C>A , CM000668.2:g.157201057C>A	GRCh38
NC_000006.11:g.157522191C>A , CM000668.1:g.157522191C>A	GRCh37
NC_000006.10:g.157563883C>A	NCBI36
NG_032093.1:g.428128C>A
NG_032093.2:g.428128C>A
NG_066624.1:g.430032C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4673C>A	ENSP00000055163.8:p.Pro1558His
ENST00000414678.8:c.4742C>A	ENSP00000412835.3:p.Pro1581His
ENST00000637015.2:c.4961C>A	ENSP00000489729.2:p.Pro1654His
ENST00000346085.10:c.4712C>A	ENSP00000344546.5:p.Pro1571His
ENST00000350026.10:c.4424C>A	ENSP00000055163.7:p.Pro1475His
ENST00000414678.7:c.2990C>A	ENSP00000412835.2:p.Pro997His
ENST00000635849.1:c.2153C>A	ENSP00000490948.1:p.Pro718His
ENST00000635957.1:c.1784C>A	ENSP00000490385.1:p.Pro595His
ENST00000636227.1:n.3295C>A
ENST00000636254.1:n.752C>A
ENST00000636930.2:c.4832C>A MANE Select	ENSP00000490491.2:p.Pro1611His
ENST00000636940.1:n.2829C>A
ENST00000637015.1:c.2200C>A
ENST00000637568.1:c.2114C>A
ENST00000637741.1:n.1498C>A
ENST00000637810.1:c.2174C>A	ENSP00000489636.1:p.Pro725His
ENST00000637904.1:c.2333C>A	ENSP00000490550.1:p.Pro778His
ENST00000647938.1:c.4463C>A	ENSP00000498155.1:p.Pro1488His
ENST00000346085.9:c.4463C>A	ENSP00000344546.4:p.Pro1488His
ENST00000350026.9:c.4424C>A	ENSP00000055163.7:p.Pro1475His
ENST00000414678.6:c.2990C>A	ENSP00000412835.2:p.Pro997His
NM_017519.2:c.4424C>A	NP_059989.2:p.Pro1475His
NM_020732.3:c.4463C>A	NP_065783.3:p.Pro1488His
XM_005267069.3:c.4583C>A	XP_005267126.2:p.Pro1528His
XM_011535984.1:c.3662C>A	XP_011534286.1:p.Pro1221His
XM_011535985.1:c.3482C>A	XP_011534287.1:p.Pro1161His
XM_011535986.1:c.3242C>A	XP_011534288.1:p.Pro1081His
XM_011535987.1:c.2861C>A	XP_011534289.1:p.Pro954His
XM_011535988.1:c.1724C>A	XP_011534290.1:p.Pro575His
NM_001346813.1:c.4583C>A	NP_001333742.1:p.Pro1528His
NM_001363725.1:c.2333C>A	NP_001350654.1:p.Pro778His
XM_011535984.2:c.4793C>A	XP_011534286.2:p.Pro1598His
XM_011535988.3:c.1724C>A	XP_011534290.1:p.Pro575His
XM_017011103.2:c.4694C>A	XP_016866592.1:p.Pro1565His
XM_017011104.1:c.4664C>A	XP_016866593.1:p.Pro1555His
XM_017011105.2:c.4634C>A	XP_016866594.1:p.Pro1545His
XM_017011106.2:c.4505C>A	XP_016866595.1:p.Pro1502His
XM_017011107.2:c.4484C>A	XP_016866596.1:p.Pro1495His
XR_002956289.1:n.4779C>A
NM_001363725.2:c.2333C>A	NP_001350654.1:p.Pro778His
NM_001371656.1:c.4712C>A	NP_001358585.1:p.Pro1571His
NM_001374820.1:c.4712C>A	NP_001361749.1:p.Pro1571His
NM_001374828.1:c.4832C>A MANE Select	NP_001361757.1:p.Pro1611His
NM_017519.3:c.4673C>A	NP_059989.3:p.Pro1558His