Canonical Allele Identifier: CA366241562

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522157A>T (hg19) ; chr6:g.157201023A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201023A>T , CM000668.2:g.157201023A>T	GRCh38
NC_000006.11:g.157522157A>T , CM000668.1:g.157522157A>T	GRCh37
NC_000006.10:g.157563849A>T	NCBI36
NG_032093.1:g.428094A>T
NG_032093.2:g.428094A>T
NG_066624.1:g.429998A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4639A>T	ENSP00000055163.8:p.Asn1547Tyr
ENST00000414678.8:c.4708A>T	ENSP00000412835.3:p.Asn1570Tyr
ENST00000637015.2:c.4927A>T	ENSP00000489729.2:p.Asn1643Tyr
ENST00000346085.10:c.4678A>T	ENSP00000344546.5:p.Asn1560Tyr
ENST00000350026.10:c.4390A>T	ENSP00000055163.7:p.Asn1464Tyr
ENST00000414678.7:c.2956A>T	ENSP00000412835.2:p.Asn986Tyr
ENST00000635849.1:c.2119A>T	ENSP00000490948.1:p.Asn707Tyr
ENST00000635957.1:c.1750A>T	ENSP00000490385.1:p.Asn584Tyr
ENST00000636227.1:n.3261A>T
ENST00000636254.1:n.718A>T
ENST00000636930.2:c.4798A>T MANE Select	ENSP00000490491.2:p.Asn1600Tyr
ENST00000636940.1:n.2795A>T
ENST00000637015.1:c.2166A>T
ENST00000637568.1:c.2080A>T
ENST00000637741.1:n.1464A>T
ENST00000637810.1:c.2140A>T	ENSP00000489636.1:p.Asn714Tyr
ENST00000637904.1:c.2299A>T	ENSP00000490550.1:p.Asn767Tyr
ENST00000647938.1:c.4429A>T	ENSP00000498155.1:p.Asn1477Tyr
ENST00000346085.9:c.4429A>T	ENSP00000344546.4:p.Asn1477Tyr
ENST00000350026.9:c.4390A>T	ENSP00000055163.7:p.Asn1464Tyr
ENST00000414678.6:c.2956A>T	ENSP00000412835.2:p.Asn986Tyr
NM_017519.2:c.4390A>T	NP_059989.2:p.Asn1464Tyr
NM_020732.3:c.4429A>T	NP_065783.3:p.Asn1477Tyr
XM_005267069.3:c.4549A>T	XP_005267126.2:p.Asn1517Tyr
XM_011535984.1:c.3628A>T	XP_011534286.1:p.Asn1210Tyr
XM_011535985.1:c.3448A>T	XP_011534287.1:p.Asn1150Tyr
XM_011535986.1:c.3208A>T	XP_011534288.1:p.Asn1070Tyr
XM_011535987.1:c.2827A>T	XP_011534289.1:p.Asn943Tyr
XM_011535988.1:c.1690A>T	XP_011534290.1:p.Asn564Tyr
NM_001346813.1:c.4549A>T	NP_001333742.1:p.Asn1517Tyr
NM_001363725.1:c.2299A>T	NP_001350654.1:p.Asn767Tyr
XM_011535984.2:c.4759A>T	XP_011534286.2:p.Asn1587Tyr
XM_011535988.3:c.1690A>T	XP_011534290.1:p.Asn564Tyr
XM_017011103.2:c.4660A>T	XP_016866592.1:p.Asn1554Tyr
XM_017011104.1:c.4630A>T	XP_016866593.1:p.Asn1544Tyr
XM_017011105.2:c.4600A>T	XP_016866594.1:p.Asn1534Tyr
XM_017011106.2:c.4471A>T	XP_016866595.1:p.Asn1491Tyr
XM_017011107.2:c.4450A>T	XP_016866596.1:p.Asn1484Tyr
XR_002956289.1:n.4745A>T
NM_001363725.2:c.2299A>T	NP_001350654.1:p.Asn767Tyr
NM_001371656.1:c.4678A>T	NP_001358585.1:p.Asn1560Tyr
NM_001374820.1:c.4678A>T	NP_001361749.1:p.Asn1560Tyr
NM_001374828.1:c.4798A>T MANE Select	NP_001361757.1:p.Asn1600Tyr
NM_017519.3:c.4639A>T	NP_059989.3:p.Asn1547Tyr