Canonical Allele Identifier: CA366242124

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522287A>T (hg19) ; chr6:g.157201153A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201153A>T , CM000668.2:g.157201153A>T	GRCh38
NC_000006.11:g.157522287A>T , CM000668.1:g.157522287A>T	GRCh37
NC_000006.10:g.157563979A>T	NCBI36
NG_032093.1:g.428224A>T
NG_032093.2:g.428224A>T
NG_066624.1:g.430128A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4769A>T	ENSP00000055163.8:p.Gln1590Leu
ENST00000414678.8:c.4838A>T	ENSP00000412835.3:p.Gln1613Leu
ENST00000637015.2:c.5057A>T	ENSP00000489729.2:p.Gln1686Leu
ENST00000346085.10:c.4808A>T	ENSP00000344546.5:p.Gln1603Leu
ENST00000350026.10:c.4520A>T	ENSP00000055163.7:p.Gln1507Leu
ENST00000414678.7:c.3086A>T	ENSP00000412835.2:p.Gln1029Leu
ENST00000635849.1:c.2249A>T	ENSP00000490948.1:p.Gln750Leu
ENST00000635957.1:c.1880A>T	ENSP00000490385.1:p.Gln627Leu
ENST00000636227.1:n.3391A>T
ENST00000636254.1:n.848A>T
ENST00000636930.2:c.4928A>T MANE Select	ENSP00000490491.2:p.Gln1643Leu
ENST00000636940.1:n.2925A>T
ENST00000637015.1:c.2296A>T
ENST00000637568.1:c.2210A>T
ENST00000637741.1:n.1594A>T
ENST00000637810.1:c.2270A>T	ENSP00000489636.1:p.Gln757Leu
ENST00000637904.1:c.2429A>T	ENSP00000490550.1:p.Gln810Leu
ENST00000647938.1:c.4559A>T	ENSP00000498155.1:p.Gln1520Leu
ENST00000346085.9:c.4559A>T	ENSP00000344546.4:p.Gln1520Leu
ENST00000350026.9:c.4520A>T	ENSP00000055163.7:p.Gln1507Leu
ENST00000414678.6:c.3086A>T	ENSP00000412835.2:p.Gln1029Leu
NM_017519.2:c.4520A>T	NP_059989.2:p.Gln1507Leu
NM_020732.3:c.4559A>T	NP_065783.3:p.Gln1520Leu
XM_005267069.3:c.4679A>T	XP_005267126.2:p.Gln1560Leu
XM_011535984.1:c.3758A>T	XP_011534286.1:p.Gln1253Leu
XM_011535985.1:c.3578A>T	XP_011534287.1:p.Gln1193Leu
XM_011535986.1:c.3338A>T	XP_011534288.1:p.Gln1113Leu
XM_011535987.1:c.2957A>T	XP_011534289.1:p.Gln986Leu
XM_011535988.1:c.1820A>T	XP_011534290.1:p.Gln607Leu
NM_001346813.1:c.4679A>T	NP_001333742.1:p.Gln1560Leu
NM_001363725.1:c.2429A>T	NP_001350654.1:p.Gln810Leu
XM_011535984.2:c.4889A>T	XP_011534286.2:p.Gln1630Leu
XM_011535988.3:c.1820A>T	XP_011534290.1:p.Gln607Leu
XM_017011103.2:c.4790A>T	XP_016866592.1:p.Gln1597Leu
XM_017011104.1:c.4760A>T	XP_016866593.1:p.Gln1587Leu
XM_017011105.2:c.4730A>T	XP_016866594.1:p.Gln1577Leu
XM_017011106.2:c.4601A>T	XP_016866595.1:p.Gln1534Leu
XM_017011107.2:c.4580A>T	XP_016866596.1:p.Gln1527Leu
XR_002956289.1:n.4875A>T
NM_001363725.2:c.2429A>T	NP_001350654.1:p.Gln810Leu
NM_001371656.1:c.4808A>T	NP_001358585.1:p.Gln1603Leu
NM_001374820.1:c.4808A>T	NP_001361749.1:p.Gln1603Leu
NM_001374828.1:c.4928A>T MANE Select	NP_001361757.1:p.Gln1643Leu
NM_017519.3:c.4769A>T	NP_059989.3:p.Gln1590Leu