Canonical Allele Identifier: CA366235239

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511231A>T (hg19) ; chr6:g.157190097A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190097A>T , CM000668.2:g.157190097A>T	GRCh38
NC_000006.11:g.157511231A>T , CM000668.1:g.157511231A>T	GRCh37
NC_000006.10:g.157552923A>T	NCBI36
NG_032093.1:g.417168A>T
NG_032093.2:g.417168A>T
NG_066624.1:g.419072A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3959A>T	ENSP00000055163.8:p.Lys1320Ile
ENST00000414678.8:c.4028A>T	ENSP00000412835.3:p.Lys1343Ile
ENST00000637015.2:c.4247A>T	ENSP00000489729.2:p.Lys1416Ile
ENST00000346085.10:c.3998A>T	ENSP00000344546.5:p.Lys1333Ile
ENST00000350026.10:c.3710A>T	ENSP00000055163.7:p.Lys1237Ile
ENST00000414678.7:c.2276A>T	ENSP00000412835.2:p.Lys759Ile
ENST00000635849.1:c.1439A>T	ENSP00000490948.1:p.Lys480Ile
ENST00000635957.1:c.1070A>T	ENSP00000490385.1:p.Lys357Ile
ENST00000636930.2:c.4118A>T MANE Select	ENSP00000490491.2:p.Lys1373Ile
ENST00000636940.1:n.2115A>T
ENST00000637015.1:c.1486A>T
ENST00000637568.1:c.1400A>T
ENST00000637741.1:n.784A>T
ENST00000637810.1:c.1460A>T	ENSP00000489636.1:p.Lys487Ile
ENST00000637904.1:c.1619A>T	ENSP00000490550.1:p.Lys540Ile
ENST00000647938.1:c.3749A>T	ENSP00000498155.1:p.Lys1250Ile
ENST00000346085.9:c.3749A>T	ENSP00000344546.4:p.Lys1250Ile
ENST00000350026.9:c.3710A>T	ENSP00000055163.7:p.Lys1237Ile
ENST00000414678.6:c.2276A>T	ENSP00000412835.2:p.Lys759Ile
NM_017519.2:c.3710A>T	NP_059989.2:p.Lys1237Ile
NM_020732.3:c.3749A>T	NP_065783.3:p.Lys1250Ile
XM_005267069.3:c.3869A>T	XP_005267126.2:p.Lys1290Ile
XM_011535984.1:c.2948A>T	XP_011534286.1:p.Lys983Ile
XM_011535985.1:c.2768A>T	XP_011534287.1:p.Lys923Ile
XM_011535986.1:c.2528A>T	XP_011534288.1:p.Lys843Ile
XM_011535987.1:c.2147A>T	XP_011534289.1:p.Lys716Ile
XM_011535988.1:c.1010A>T	XP_011534290.1:p.Lys337Ile
NM_001346813.1:c.3869A>T	NP_001333742.1:p.Lys1290Ile
NM_001363725.1:c.1619A>T	NP_001350654.1:p.Lys540Ile
XM_011535984.2:c.4079A>T	XP_011534286.2:p.Lys1360Ile
XM_011535988.3:c.1010A>T	XP_011534290.1:p.Lys337Ile
XM_017011103.2:c.3980A>T	XP_016866592.1:p.Lys1327Ile
XM_017011104.1:c.3950A>T	XP_016866593.1:p.Lys1317Ile
XM_017011105.2:c.3920A>T	XP_016866594.1:p.Lys1307Ile
XM_017011106.2:c.3791A>T	XP_016866595.1:p.Lys1264Ile
XM_017011107.2:c.3770A>T	XP_016866596.1:p.Lys1257Ile
XR_002956289.1:n.4162A>T
NM_001363725.2:c.1619A>T	NP_001350654.1:p.Lys540Ile
NM_001371656.1:c.3998A>T	NP_001358585.1:p.Lys1333Ile
NM_001374820.1:c.3998A>T	NP_001361749.1:p.Lys1333Ile
NM_001374828.1:c.4118A>T MANE Select	NP_001361757.1:p.Lys1373Ile
NM_017519.3:c.3959A>T	NP_059989.3:p.Lys1320Ile