Canonical Allele Identifier: CA366239476

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128365947
• MyVariant Identifiers: chr6:g.157519950A>T (hg19) ; chr6:g.157198816A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198816A>T , CM000668.2:g.157198816A>T	GRCh38
NC_000006.11:g.157519950A>T , CM000668.1:g.157519950A>T	GRCh37
NC_000006.10:g.157561642A>T	NCBI36
NG_032093.1:g.425887A>T
NG_032093.2:g.425887A>T
NG_066624.1:g.427791A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4229A>T	ENSP00000055163.8:p.Glu1410Val
ENST00000414678.8:c.4298A>T	ENSP00000412835.3:p.Glu1433Val
ENST00000637015.2:c.4517A>T	ENSP00000489729.2:p.Glu1506Val
ENST00000346085.10:c.4268A>T	ENSP00000344546.5:p.Glu1423Val
ENST00000350026.10:c.3980A>T	ENSP00000055163.7:p.Glu1327Val
ENST00000414678.7:c.2546A>T	ENSP00000412835.2:p.Glu849Val
ENST00000635849.1:c.1709A>T	ENSP00000490948.1:p.Glu570Val
ENST00000635957.1:c.1340A>T	ENSP00000490385.1:p.Glu447Val
ENST00000636227.1:n.2851A>T
ENST00000636254.1:n.308A>T
ENST00000636930.2:c.4388A>T MANE Select	ENSP00000490491.2:p.Glu1463Val
ENST00000636940.1:n.2385A>T
ENST00000637015.1:c.1756A>T
ENST00000637568.1:c.1670A>T
ENST00000637741.1:n.1054A>T
ENST00000637810.1:c.1730A>T	ENSP00000489636.1:p.Glu577Val
ENST00000637904.1:c.1889A>T	ENSP00000490550.1:p.Glu630Val
ENST00000647938.1:c.4019A>T	ENSP00000498155.1:p.Glu1340Val
ENST00000346085.9:c.4019A>T	ENSP00000344546.4:p.Glu1340Val
ENST00000350026.9:c.3980A>T	ENSP00000055163.7:p.Glu1327Val
ENST00000414678.6:c.2546A>T	ENSP00000412835.2:p.Glu849Val
NM_017519.2:c.3980A>T	NP_059989.2:p.Glu1327Val
NM_020732.3:c.4019A>T	NP_065783.3:p.Glu1340Val
XM_005267069.3:c.4139A>T	XP_005267126.2:p.Glu1380Val
XM_011535984.1:c.3218A>T	XP_011534286.1:p.Glu1073Val
XM_011535985.1:c.3038A>T	XP_011534287.1:p.Glu1013Val
XM_011535986.1:c.2798A>T	XP_011534288.1:p.Glu933Val
XM_011535987.1:c.2417A>T	XP_011534289.1:p.Glu806Val
XM_011535988.1:c.1280A>T	XP_011534290.1:p.Glu427Val
NM_001346813.1:c.4139A>T	NP_001333742.1:p.Glu1380Val
NM_001363725.1:c.1889A>T	NP_001350654.1:p.Glu630Val
XM_011535984.2:c.4349A>T	XP_011534286.2:p.Glu1450Val
XM_011535988.3:c.1280A>T	XP_011534290.1:p.Glu427Val
XM_017011103.2:c.4250A>T	XP_016866592.1:p.Glu1417Val
XM_017011104.1:c.4220A>T	XP_016866593.1:p.Glu1407Val
XM_017011105.2:c.4190A>T	XP_016866594.1:p.Glu1397Val
XM_017011106.2:c.4061A>T	XP_016866595.1:p.Glu1354Val
XM_017011107.2:c.4040A>T	XP_016866596.1:p.Glu1347Val
XR_002956289.1:n.4427-1889A>T
NM_001363725.2:c.1889A>T	NP_001350654.1:p.Glu630Val
NM_001371656.1:c.4268A>T	NP_001358585.1:p.Glu1423Val
NM_001374820.1:c.4268A>T	NP_001361749.1:p.Glu1423Val
NM_001374828.1:c.4388A>T MANE Select	NP_001361757.1:p.Glu1463Val
NM_017519.3:c.4229A>T	NP_059989.3:p.Glu1410Val