Canonical Allele Identifier: CA366241552

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522156G>T (hg19) ; chr6:g.157201022G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201022G>T , CM000668.2:g.157201022G>T	GRCh38
NC_000006.11:g.157522156G>T , CM000668.1:g.157522156G>T	GRCh37
NC_000006.10:g.157563848G>T	NCBI36
NG_032093.1:g.428093G>T
NG_032093.2:g.428093G>T
NG_066624.1:g.429997G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4638G>T	ENSP00000055163.8:p.Gln1546His
ENST00000414678.8:c.4707G>T	ENSP00000412835.3:p.Gln1569His
ENST00000637015.2:c.4926G>T	ENSP00000489729.2:p.Gln1642His
ENST00000346085.10:c.4677G>T	ENSP00000344546.5:p.Gln1559His
ENST00000350026.10:c.4389G>T	ENSP00000055163.7:p.Gln1463His
ENST00000414678.7:c.2955G>T	ENSP00000412835.2:p.Gln985His
ENST00000635849.1:c.2118G>T	ENSP00000490948.1:p.Gln706His
ENST00000635957.1:c.1749G>T	ENSP00000490385.1:p.Gln583His
ENST00000636227.1:n.3260G>T
ENST00000636254.1:n.717G>T
ENST00000636930.2:c.4797G>T MANE Select	ENSP00000490491.2:p.Gln1599His
ENST00000636940.1:n.2794G>T
ENST00000637015.1:c.2165G>T
ENST00000637568.1:c.2079G>T
ENST00000637741.1:n.1463G>T
ENST00000637810.1:c.2139G>T	ENSP00000489636.1:p.Gln713His
ENST00000637904.1:c.2298G>T	ENSP00000490550.1:p.Gln766His
ENST00000647938.1:c.4428G>T	ENSP00000498155.1:p.Gln1476His
ENST00000346085.9:c.4428G>T	ENSP00000344546.4:p.Gln1476His
ENST00000350026.9:c.4389G>T	ENSP00000055163.7:p.Gln1463His
ENST00000414678.6:c.2955G>T	ENSP00000412835.2:p.Gln985His
NM_017519.2:c.4389G>T	NP_059989.2:p.Gln1463His
NM_020732.3:c.4428G>T	NP_065783.3:p.Gln1476His
XM_005267069.3:c.4548G>T	XP_005267126.2:p.Gln1516His
XM_011535984.1:c.3627G>T	XP_011534286.1:p.Gln1209His
XM_011535985.1:c.3447G>T	XP_011534287.1:p.Gln1149His
XM_011535986.1:c.3207G>T	XP_011534288.1:p.Gln1069His
XM_011535987.1:c.2826G>T	XP_011534289.1:p.Gln942His
XM_011535988.1:c.1689G>T	XP_011534290.1:p.Gln563His
NM_001346813.1:c.4548G>T	NP_001333742.1:p.Gln1516His
NM_001363725.1:c.2298G>T	NP_001350654.1:p.Gln766His
XM_011535984.2:c.4758G>T	XP_011534286.2:p.Gln1586His
XM_011535988.3:c.1689G>T	XP_011534290.1:p.Gln563His
XM_017011103.2:c.4659G>T	XP_016866592.1:p.Gln1553His
XM_017011104.1:c.4629G>T	XP_016866593.1:p.Gln1543His
XM_017011105.2:c.4599G>T	XP_016866594.1:p.Gln1533His
XM_017011106.2:c.4470G>T	XP_016866595.1:p.Gln1490His
XM_017011107.2:c.4449G>T	XP_016866596.1:p.Gln1483His
XR_002956289.1:n.4744G>T
NM_001363725.2:c.2298G>T	NP_001350654.1:p.Gln766His
NM_001371656.1:c.4677G>T	NP_001358585.1:p.Gln1559His
NM_001374820.1:c.4677G>T	NP_001361749.1:p.Gln1559His
NM_001374828.1:c.4797G>T MANE Select	NP_001361757.1:p.Gln1599His
NM_017519.3:c.4638G>T	NP_059989.3:p.Gln1546His