Canonical Allele Identifier: CA366241352

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522111G>T (hg19) ; chr6:g.157200977G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200977G>T , CM000668.2:g.157200977G>T	GRCh38
NC_000006.11:g.157522111G>T , CM000668.1:g.157522111G>T	GRCh37
NC_000006.10:g.157563803G>T	NCBI36
NG_032093.1:g.428048G>T
NG_032093.2:g.428048G>T
NG_066624.1:g.429952G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4593G>T	ENSP00000055163.8:p.Gln1531His
ENST00000414678.8:c.4662G>T	ENSP00000412835.3:p.Gln1554His
ENST00000637015.2:c.4881G>T	ENSP00000489729.2:p.Gln1627His
ENST00000346085.10:c.4632G>T	ENSP00000344546.5:p.Gln1544His
ENST00000350026.10:c.4344G>T	ENSP00000055163.7:p.Gln1448His
ENST00000414678.7:c.2910G>T	ENSP00000412835.2:p.Gln970His
ENST00000635849.1:c.2073G>T	ENSP00000490948.1:p.Gln691His
ENST00000635957.1:c.1704G>T	ENSP00000490385.1:p.Gln568His
ENST00000636227.1:n.3215G>T
ENST00000636254.1:n.672G>T
ENST00000636930.2:c.4752G>T MANE Select	ENSP00000490491.2:p.Gln1584His
ENST00000636940.1:n.2749G>T
ENST00000637015.1:c.2120G>T
ENST00000637568.1:c.2034G>T
ENST00000637741.1:n.1418G>T
ENST00000637810.1:c.2094G>T	ENSP00000489636.1:p.Gln698His
ENST00000637904.1:c.2253G>T	ENSP00000490550.1:p.Gln751His
ENST00000647938.1:c.4383G>T	ENSP00000498155.1:p.Gln1461His
ENST00000346085.9:c.4383G>T	ENSP00000344546.4:p.Gln1461His
ENST00000350026.9:c.4344G>T	ENSP00000055163.7:p.Gln1448His
ENST00000414678.6:c.2910G>T	ENSP00000412835.2:p.Gln970His
NM_017519.2:c.4344G>T	NP_059989.2:p.Gln1448His
NM_020732.3:c.4383G>T	NP_065783.3:p.Gln1461His
XM_005267069.3:c.4503G>T	XP_005267126.2:p.Gln1501His
XM_011535984.1:c.3582G>T	XP_011534286.1:p.Gln1194His
XM_011535985.1:c.3402G>T	XP_011534287.1:p.Gln1134His
XM_011535986.1:c.3162G>T	XP_011534288.1:p.Gln1054His
XM_011535987.1:c.2781G>T	XP_011534289.1:p.Gln927His
XM_011535988.1:c.1644G>T	XP_011534290.1:p.Gln548His
NM_001346813.1:c.4503G>T	NP_001333742.1:p.Gln1501His
NM_001363725.1:c.2253G>T	NP_001350654.1:p.Gln751His
XM_011535984.2:c.4713G>T	XP_011534286.2:p.Gln1571His
XM_011535988.3:c.1644G>T	XP_011534290.1:p.Gln548His
XM_017011103.2:c.4614G>T	XP_016866592.1:p.Gln1538His
XM_017011104.1:c.4584G>T	XP_016866593.1:p.Gln1528His
XM_017011105.2:c.4554G>T	XP_016866594.1:p.Gln1518His
XM_017011106.2:c.4425G>T	XP_016866595.1:p.Gln1475His
XM_017011107.2:c.4404G>T	XP_016866596.1:p.Gln1468His
XR_002956289.1:n.4699G>T
NM_001363725.2:c.2253G>T	NP_001350654.1:p.Gln751His
NM_001371656.1:c.4632G>T	NP_001358585.1:p.Gln1544His
NM_001374820.1:c.4632G>T	NP_001361749.1:p.Gln1544His
NM_001374828.1:c.4752G>T MANE Select	NP_001361757.1:p.Gln1584His
NM_017519.3:c.4593G>T	NP_059989.3:p.Gln1531His