Canonical Allele Identifier: CA366241312

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522094T>C (hg19) ; chr6:g.157200960T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200960T>C , CM000668.2:g.157200960T>C	GRCh38
NC_000006.11:g.157522094T>C , CM000668.1:g.157522094T>C	GRCh37
NC_000006.10:g.157563786T>C	NCBI36
NG_032093.1:g.428031T>C
NG_032093.2:g.428031T>C
NG_066624.1:g.429935T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4576T>C	ENSP00000055163.8:p.Ser1526Pro
ENST00000414678.8:c.4645T>C	ENSP00000412835.3:p.Ser1549Pro
ENST00000637015.2:c.4864T>C	ENSP00000489729.2:p.Ser1622Pro
ENST00000346085.10:c.4615T>C	ENSP00000344546.5:p.Ser1539Pro
ENST00000350026.10:c.4327T>C	ENSP00000055163.7:p.Ser1443Pro
ENST00000414678.7:c.2893T>C	ENSP00000412835.2:p.Ser965Pro
ENST00000635849.1:c.2056T>C	ENSP00000490948.1:p.Ser686Pro
ENST00000635957.1:c.1687T>C	ENSP00000490385.1:p.Ser563Pro
ENST00000636227.1:n.3198T>C
ENST00000636254.1:n.655T>C
ENST00000636930.2:c.4735T>C MANE Select	ENSP00000490491.2:p.Ser1579Pro
ENST00000636940.1:n.2732T>C
ENST00000637015.1:c.2103T>C
ENST00000637568.1:c.2017T>C
ENST00000637741.1:n.1401T>C
ENST00000637810.1:c.2077T>C	ENSP00000489636.1:p.Ser693Pro
ENST00000637904.1:c.2236T>C	ENSP00000490550.1:p.Ser746Pro
ENST00000647938.1:c.4366T>C	ENSP00000498155.1:p.Ser1456Pro
ENST00000346085.9:c.4366T>C	ENSP00000344546.4:p.Ser1456Pro
ENST00000350026.9:c.4327T>C	ENSP00000055163.7:p.Ser1443Pro
ENST00000414678.6:c.2893T>C	ENSP00000412835.2:p.Ser965Pro
NM_017519.2:c.4327T>C	NP_059989.2:p.Ser1443Pro
NM_020732.3:c.4366T>C	NP_065783.3:p.Ser1456Pro
XM_005267069.3:c.4486T>C	XP_005267126.2:p.Ser1496Pro
XM_011535984.1:c.3565T>C	XP_011534286.1:p.Ser1189Pro
XM_011535985.1:c.3385T>C	XP_011534287.1:p.Ser1129Pro
XM_011535986.1:c.3145T>C	XP_011534288.1:p.Ser1049Pro
XM_011535987.1:c.2764T>C	XP_011534289.1:p.Ser922Pro
XM_011535988.1:c.1627T>C	XP_011534290.1:p.Ser543Pro
NM_001346813.1:c.4486T>C	NP_001333742.1:p.Ser1496Pro
NM_001363725.1:c.2236T>C	NP_001350654.1:p.Ser746Pro
XM_011535984.2:c.4696T>C	XP_011534286.2:p.Ser1566Pro
XM_011535988.3:c.1627T>C	XP_011534290.1:p.Ser543Pro
XM_017011103.2:c.4597T>C	XP_016866592.1:p.Ser1533Pro
XM_017011104.1:c.4567T>C	XP_016866593.1:p.Ser1523Pro
XM_017011105.2:c.4537T>C	XP_016866594.1:p.Ser1513Pro
XM_017011106.2:c.4408T>C	XP_016866595.1:p.Ser1470Pro
XM_017011107.2:c.4387T>C	XP_016866596.1:p.Ser1463Pro
XR_002956289.1:n.4682T>C
NM_001363725.2:c.2236T>C	NP_001350654.1:p.Ser746Pro
NM_001371656.1:c.4615T>C	NP_001358585.1:p.Ser1539Pro
NM_001374820.1:c.4615T>C	NP_001361749.1:p.Ser1539Pro
NM_001374828.1:c.4735T>C MANE Select	NP_001361757.1:p.Ser1579Pro
NM_017519.3:c.4576T>C	NP_059989.3:p.Ser1526Pro