Canonical Allele Identifier: CA452978421

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374397
• MyVariant Identifiers: chr6:g.157522210C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201076C>T , CM000668.2:g.157201076C>T	GRCh38
NC_000006.11:g.157522210C>T , CM000668.1:g.157522210C>T	GRCh37
NC_000006.10:g.157563902C>T	NCBI36
NG_032093.1:g.428147C>T
NG_032093.2:g.428147C>T
NG_066624.1:g.430051C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4692C>T	ENSP00000055163.8:p.Asn1564=
ENST00000414678.8:c.4761C>T	ENSP00000412835.3:p.Asn1587=
ENST00000637015.2:c.4980C>T	ENSP00000489729.2:p.Asn1660=
ENST00000346085.10:c.4731C>T	ENSP00000344546.5:p.Asn1577=
ENST00000350026.10:c.4443C>T	ENSP00000055163.7:p.Asn1481=
ENST00000414678.7:c.3009C>T	ENSP00000412835.2:p.Asn1003=
ENST00000635849.1:c.2172C>T	ENSP00000490948.1:p.Asn724=
ENST00000635957.1:c.1803C>T	ENSP00000490385.1:p.Asn601=
ENST00000636227.1:n.3314C>T
ENST00000636254.1:n.771C>T
ENST00000636930.2:c.4851C>T MANE Select	ENSP00000490491.2:p.Asn1617=
ENST00000636940.1:n.2848C>T
ENST00000637015.1:c.2219C>T
ENST00000637568.1:c.2133C>T
ENST00000637741.1:n.1517C>T
ENST00000637810.1:c.2193C>T	ENSP00000489636.1:p.Asn731=
ENST00000637904.1:c.2352C>T	ENSP00000490550.1:p.Asn784=
ENST00000647938.1:c.4482C>T	ENSP00000498155.1:p.Asn1494=
ENST00000346085.9:c.4482C>T	ENSP00000344546.4:p.Asn1494=
ENST00000350026.9:c.4443C>T	ENSP00000055163.7:p.Asn1481=
ENST00000414678.6:c.3009C>T	ENSP00000412835.2:p.Asn1003=
NM_017519.2:c.4443C>T	NP_059989.2:p.Asn1481=
NM_020732.3:c.4482C>T	NP_065783.3:p.Asn1494=
XM_005267069.3:c.4602C>T	XP_005267126.2:p.Asn1534=
XM_011535984.1:c.3681C>T	XP_011534286.1:p.Asn1227=
XM_011535985.1:c.3501C>T	XP_011534287.1:p.Asn1167=
XM_011535986.1:c.3261C>T	XP_011534288.1:p.Asn1087=
XM_011535987.1:c.2880C>T	XP_011534289.1:p.Asn960=
XM_011535988.1:c.1743C>T	XP_011534290.1:p.Asn581=
NM_001346813.1:c.4602C>T	NP_001333742.1:p.Asn1534=
NM_001363725.1:c.2352C>T	NP_001350654.1:p.Asn784=
XM_011535984.2:c.4812C>T	XP_011534286.2:p.Asn1604=
XM_011535988.3:c.1743C>T	XP_011534290.1:p.Asn581=
XM_017011103.2:c.4713C>T	XP_016866592.1:p.Asn1571=
XM_017011104.1:c.4683C>T	XP_016866593.1:p.Asn1561=
XM_017011105.2:c.4653C>T	XP_016866594.1:p.Asn1551=
XM_017011106.2:c.4524C>T	XP_016866595.1:p.Asn1508=
XM_017011107.2:c.4503C>T	XP_016866596.1:p.Asn1501=
XR_002956289.1:n.4798C>T
NM_001363725.2:c.2352C>T	NP_001350654.1:p.Asn784=
NM_001371656.1:c.4731C>T	NP_001358585.1:p.Asn1577=
NM_001374820.1:c.4731C>T	NP_001361749.1:p.Asn1577=
NM_001374828.1:c.4851C>T MANE Select	NP_001361757.1:p.Asn1617=
NM_017519.3:c.4692C>T	NP_059989.3:p.Asn1564=