Canonical Allele Identifier: CA366241847

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1683799
• ClinVar RCV Id: RCV002244321
• dbSNP Id: rs2128374397
• MyVariant Identifiers: chr6:g.157522210C>A (hg19) ; chr6:g.157201076C>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4692C>A	ENSP00000055163.8:p.Asn1564Lys
ENST00000414678.8:c.4761C>A	ENSP00000412835.3:p.Asn1587Lys
ENST00000637015.2:c.4980C>A	ENSP00000489729.2:p.Asn1660Lys
ENST00000346085.10:c.4731C>A	ENSP00000344546.5:p.Asn1577Lys
ENST00000350026.10:c.4443C>A	ENSP00000055163.7:p.Asn1481Lys
ENST00000414678.7:c.3009C>A	ENSP00000412835.2:p.Asn1003Lys
ENST00000635849.1:c.2172C>A	ENSP00000490948.1:p.Asn724Lys
ENST00000635957.1:c.1803C>A	ENSP00000490385.1:p.Asn601Lys
ENST00000636227.1:n.3314C>A
ENST00000636254.1:n.771C>A
ENST00000636930.2:c.4851C>A MANE Select	ENSP00000490491.2:p.Asn1617Lys
ENST00000636940.1:n.2848C>A
ENST00000637015.1:c.2219C>A
ENST00000637568.1:c.2133C>A
ENST00000637741.1:n.1517C>A
ENST00000637810.1:c.2193C>A	ENSP00000489636.1:p.Asn731Lys
ENST00000637904.1:c.2352C>A	ENSP00000490550.1:p.Asn784Lys
ENST00000647938.1:c.4482C>A	ENSP00000498155.1:p.Asn1494Lys
ENST00000346085.9:c.4482C>A	ENSP00000344546.4:p.Asn1494Lys
ENST00000350026.9:c.4443C>A	ENSP00000055163.7:p.Asn1481Lys
ENST00000414678.6:c.3009C>A	ENSP00000412835.2:p.Asn1003Lys
NM_017519.2:c.4443C>A	NP_059989.2:p.Asn1481Lys
NM_020732.3:c.4482C>A	NP_065783.3:p.Asn1494Lys
XM_005267069.3:c.4602C>A	XP_005267126.2:p.Asn1534Lys
XM_011535984.1:c.3681C>A	XP_011534286.1:p.Asn1227Lys
XM_011535985.1:c.3501C>A	XP_011534287.1:p.Asn1167Lys
XM_011535986.1:c.3261C>A	XP_011534288.1:p.Asn1087Lys
XM_011535987.1:c.2880C>A	XP_011534289.1:p.Asn960Lys
XM_011535988.1:c.1743C>A	XP_011534290.1:p.Asn581Lys
NM_001346813.1:c.4602C>A	NP_001333742.1:p.Asn1534Lys
NM_001363725.1:c.2352C>A	NP_001350654.1:p.Asn784Lys
XM_011535984.2:c.4812C>A	XP_011534286.2:p.Asn1604Lys
XM_011535988.3:c.1743C>A	XP_011534290.1:p.Asn581Lys
XM_017011103.2:c.4713C>A	XP_016866592.1:p.Asn1571Lys
XM_017011104.1:c.4683C>A	XP_016866593.1:p.Asn1561Lys
XM_017011105.2:c.4653C>A	XP_016866594.1:p.Asn1551Lys
XM_017011106.2:c.4524C>A	XP_016866595.1:p.Asn1508Lys
XM_017011107.2:c.4503C>A	XP_016866596.1:p.Asn1501Lys
XR_002956289.1:n.4798C>A
NM_001363725.2:c.2352C>A	NP_001350654.1:p.Asn784Lys
NM_001371656.1:c.4731C>A	NP_001358585.1:p.Asn1577Lys
NM_001374820.1:c.4731C>A	NP_001361749.1:p.Asn1577Lys
NM_001374828.1:c.4851C>A MANE Select	NP_001361757.1:p.Asn1617Lys
NM_017519.3:c.4692C>A	NP_059989.3:p.Asn1564Lys