Canonical Allele Identifier: CA366241833

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374383
• MyVariant Identifiers: chr6:g.157522208A>T (hg19) ; chr6:g.157201074A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201074A>T , CM000668.2:g.157201074A>T	GRCh38
NC_000006.11:g.157522208A>T , CM000668.1:g.157522208A>T	GRCh37
NC_000006.10:g.157563900A>T	NCBI36
NG_032093.1:g.428145A>T
NG_032093.2:g.428145A>T
NG_066624.1:g.430049A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4690A>T	ENSP00000055163.8:p.Asn1564Tyr
ENST00000414678.8:c.4759A>T	ENSP00000412835.3:p.Asn1587Tyr
ENST00000637015.2:c.4978A>T	ENSP00000489729.2:p.Asn1660Tyr
ENST00000346085.10:c.4729A>T	ENSP00000344546.5:p.Asn1577Tyr
ENST00000350026.10:c.4441A>T	ENSP00000055163.7:p.Asn1481Tyr
ENST00000414678.7:c.3007A>T	ENSP00000412835.2:p.Asn1003Tyr
ENST00000635849.1:c.2170A>T	ENSP00000490948.1:p.Asn724Tyr
ENST00000635957.1:c.1801A>T	ENSP00000490385.1:p.Asn601Tyr
ENST00000636227.1:n.3312A>T
ENST00000636254.1:n.769A>T
ENST00000636930.2:c.4849A>T MANE Select	ENSP00000490491.2:p.Asn1617Tyr
ENST00000636940.1:n.2846A>T
ENST00000637015.1:c.2217A>T
ENST00000637568.1:c.2131A>T
ENST00000637741.1:n.1515A>T
ENST00000637810.1:c.2191A>T	ENSP00000489636.1:p.Asn731Tyr
ENST00000637904.1:c.2350A>T	ENSP00000490550.1:p.Asn784Tyr
ENST00000647938.1:c.4480A>T	ENSP00000498155.1:p.Asn1494Tyr
ENST00000346085.9:c.4480A>T	ENSP00000344546.4:p.Asn1494Tyr
ENST00000350026.9:c.4441A>T	ENSP00000055163.7:p.Asn1481Tyr
ENST00000414678.6:c.3007A>T	ENSP00000412835.2:p.Asn1003Tyr
NM_017519.2:c.4441A>T	NP_059989.2:p.Asn1481Tyr
NM_020732.3:c.4480A>T	NP_065783.3:p.Asn1494Tyr
XM_005267069.3:c.4600A>T	XP_005267126.2:p.Asn1534Tyr
XM_011535984.1:c.3679A>T	XP_011534286.1:p.Asn1227Tyr
XM_011535985.1:c.3499A>T	XP_011534287.1:p.Asn1167Tyr
XM_011535986.1:c.3259A>T	XP_011534288.1:p.Asn1087Tyr
XM_011535987.1:c.2878A>T	XP_011534289.1:p.Asn960Tyr
XM_011535988.1:c.1741A>T	XP_011534290.1:p.Asn581Tyr
NM_001346813.1:c.4600A>T	NP_001333742.1:p.Asn1534Tyr
NM_001363725.1:c.2350A>T	NP_001350654.1:p.Asn784Tyr
XM_011535984.2:c.4810A>T	XP_011534286.2:p.Asn1604Tyr
XM_011535988.3:c.1741A>T	XP_011534290.1:p.Asn581Tyr
XM_017011103.2:c.4711A>T	XP_016866592.1:p.Asn1571Tyr
XM_017011104.1:c.4681A>T	XP_016866593.1:p.Asn1561Tyr
XM_017011105.2:c.4651A>T	XP_016866594.1:p.Asn1551Tyr
XM_017011106.2:c.4522A>T	XP_016866595.1:p.Asn1508Tyr
XM_017011107.2:c.4501A>T	XP_016866596.1:p.Asn1501Tyr
XR_002956289.1:n.4796A>T
NM_001363725.2:c.2350A>T	NP_001350654.1:p.Asn784Tyr
NM_001371656.1:c.4729A>T	NP_001358585.1:p.Asn1577Tyr
NM_001374820.1:c.4729A>T	NP_001361749.1:p.Asn1577Tyr
NM_001374828.1:c.4849A>T MANE Select	NP_001361757.1:p.Asn1617Tyr
NM_017519.3:c.4690A>T	NP_059989.3:p.Asn1564Tyr