Canonical Allele Identifier: CA366241362

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522115A>T (hg19) ; chr6:g.157200981A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200981A>T , CM000668.2:g.157200981A>T	GRCh38
NC_000006.11:g.157522115A>T , CM000668.1:g.157522115A>T	GRCh37
NC_000006.10:g.157563807A>T	NCBI36
NG_032093.1:g.428052A>T
NG_032093.2:g.428052A>T
NG_066624.1:g.429956A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4597A>T	ENSP00000055163.8:p.Asn1533Tyr
ENST00000414678.8:c.4666A>T	ENSP00000412835.3:p.Asn1556Tyr
ENST00000637015.2:c.4885A>T	ENSP00000489729.2:p.Asn1629Tyr
ENST00000346085.10:c.4636A>T	ENSP00000344546.5:p.Asn1546Tyr
ENST00000350026.10:c.4348A>T	ENSP00000055163.7:p.Asn1450Tyr
ENST00000414678.7:c.2914A>T	ENSP00000412835.2:p.Asn972Tyr
ENST00000635849.1:c.2077A>T	ENSP00000490948.1:p.Asn693Tyr
ENST00000635957.1:c.1708A>T	ENSP00000490385.1:p.Asn570Tyr
ENST00000636227.1:n.3219A>T
ENST00000636254.1:n.676A>T
ENST00000636930.2:c.4756A>T MANE Select	ENSP00000490491.2:p.Asn1586Tyr
ENST00000636940.1:n.2753A>T
ENST00000637015.1:c.2124A>T
ENST00000637568.1:c.2038A>T
ENST00000637741.1:n.1422A>T
ENST00000637810.1:c.2098A>T	ENSP00000489636.1:p.Asn700Tyr
ENST00000637904.1:c.2257A>T	ENSP00000490550.1:p.Asn753Tyr
ENST00000647938.1:c.4387A>T	ENSP00000498155.1:p.Asn1463Tyr
ENST00000346085.9:c.4387A>T	ENSP00000344546.4:p.Asn1463Tyr
ENST00000350026.9:c.4348A>T	ENSP00000055163.7:p.Asn1450Tyr
ENST00000414678.6:c.2914A>T	ENSP00000412835.2:p.Asn972Tyr
NM_017519.2:c.4348A>T	NP_059989.2:p.Asn1450Tyr
NM_020732.3:c.4387A>T	NP_065783.3:p.Asn1463Tyr
XM_005267069.3:c.4507A>T	XP_005267126.2:p.Asn1503Tyr
XM_011535984.1:c.3586A>T	XP_011534286.1:p.Asn1196Tyr
XM_011535985.1:c.3406A>T	XP_011534287.1:p.Asn1136Tyr
XM_011535986.1:c.3166A>T	XP_011534288.1:p.Asn1056Tyr
XM_011535987.1:c.2785A>T	XP_011534289.1:p.Asn929Tyr
XM_011535988.1:c.1648A>T	XP_011534290.1:p.Asn550Tyr
NM_001346813.1:c.4507A>T	NP_001333742.1:p.Asn1503Tyr
NM_001363725.1:c.2257A>T	NP_001350654.1:p.Asn753Tyr
XM_011535984.2:c.4717A>T	XP_011534286.2:p.Asn1573Tyr
XM_011535988.3:c.1648A>T	XP_011534290.1:p.Asn550Tyr
XM_017011103.2:c.4618A>T	XP_016866592.1:p.Asn1540Tyr
XM_017011104.1:c.4588A>T	XP_016866593.1:p.Asn1530Tyr
XM_017011105.2:c.4558A>T	XP_016866594.1:p.Asn1520Tyr
XM_017011106.2:c.4429A>T	XP_016866595.1:p.Asn1477Tyr
XM_017011107.2:c.4408A>T	XP_016866596.1:p.Asn1470Tyr
XR_002956289.1:n.4703A>T
NM_001363725.2:c.2257A>T	NP_001350654.1:p.Asn753Tyr
NM_001371656.1:c.4636A>T	NP_001358585.1:p.Asn1546Tyr
NM_001374820.1:c.4636A>T	NP_001361749.1:p.Asn1546Tyr
NM_001374828.1:c.4756A>T MANE Select	NP_001361757.1:p.Asn1586Tyr
NM_017519.3:c.4597A>T	NP_059989.3:p.Asn1533Tyr