Canonical Allele Identifier: CA366241361

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4597A>G	ENSP00000055163.8:p.Asn1533Asp
ENST00000414678.8:c.4666A>G	ENSP00000412835.3:p.Asn1556Asp
ENST00000637015.2:c.4885A>G	ENSP00000489729.2:p.Asn1629Asp
ENST00000346085.10:c.4636A>G	ENSP00000344546.5:p.Asn1546Asp
ENST00000350026.10:c.4348A>G	ENSP00000055163.7:p.Asn1450Asp
ENST00000414678.7:c.2914A>G	ENSP00000412835.2:p.Asn972Asp
ENST00000635849.1:c.2077A>G	ENSP00000490948.1:p.Asn693Asp
ENST00000635957.1:c.1708A>G	ENSP00000490385.1:p.Asn570Asp
ENST00000636227.1:n.3219A>G
ENST00000636254.1:n.676A>G
ENST00000636930.2:c.4756A>G MANE Select	ENSP00000490491.2:p.Asn1586Asp
ENST00000636940.1:n.2753A>G
ENST00000637015.1:c.2124A>G
ENST00000637568.1:c.2038A>G
ENST00000637741.1:n.1422A>G
ENST00000637810.1:c.2098A>G	ENSP00000489636.1:p.Asn700Asp
ENST00000637904.1:c.2257A>G	ENSP00000490550.1:p.Asn753Asp
ENST00000647938.1:c.4387A>G	ENSP00000498155.1:p.Asn1463Asp
ENST00000346085.9:c.4387A>G	ENSP00000344546.4:p.Asn1463Asp
ENST00000350026.9:c.4348A>G	ENSP00000055163.7:p.Asn1450Asp
ENST00000414678.6:c.2914A>G	ENSP00000412835.2:p.Asn972Asp
NM_017519.2:c.4348A>G	NP_059989.2:p.Asn1450Asp
NM_020732.3:c.4387A>G	NP_065783.3:p.Asn1463Asp
XM_005267069.3:c.4507A>G	XP_005267126.2:p.Asn1503Asp
XM_011535984.1:c.3586A>G	XP_011534286.1:p.Asn1196Asp
XM_011535985.1:c.3406A>G	XP_011534287.1:p.Asn1136Asp
XM_011535986.1:c.3166A>G	XP_011534288.1:p.Asn1056Asp
XM_011535987.1:c.2785A>G	XP_011534289.1:p.Asn929Asp
XM_011535988.1:c.1648A>G	XP_011534290.1:p.Asn550Asp
NM_001346813.1:c.4507A>G	NP_001333742.1:p.Asn1503Asp
NM_001363725.1:c.2257A>G	NP_001350654.1:p.Asn753Asp
XM_011535984.2:c.4717A>G	XP_011534286.2:p.Asn1573Asp
XM_011535988.3:c.1648A>G	XP_011534290.1:p.Asn550Asp
XM_017011103.2:c.4618A>G	XP_016866592.1:p.Asn1540Asp
XM_017011104.1:c.4588A>G	XP_016866593.1:p.Asn1530Asp
XM_017011105.2:c.4558A>G	XP_016866594.1:p.Asn1520Asp
XM_017011106.2:c.4429A>G	XP_016866595.1:p.Asn1477Asp
XM_017011107.2:c.4408A>G	XP_016866596.1:p.Asn1470Asp
XR_002956289.1:n.4703A>G
NM_001363725.2:c.2257A>G	NP_001350654.1:p.Asn753Asp
NM_001371656.1:c.4636A>G	NP_001358585.1:p.Asn1546Asp
NM_001374820.1:c.4636A>G	NP_001361749.1:p.Asn1546Asp
NM_001374828.1:c.4756A>G MANE Select	NP_001361757.1:p.Asn1586Asp
NM_017519.3:c.4597A>G	NP_059989.3:p.Asn1533Asp