Canonical Allele Identifier: CA366241402

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157200997-G-T
• MyVariant Identifiers: chr6:g.157522131G>T (hg19) ; chr6:g.157200997G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200997G>T , CM000668.2:g.157200997G>T	GRCh38
NC_000006.11:g.157522131G>T , CM000668.1:g.157522131G>T	GRCh37
NC_000006.10:g.157563823G>T	NCBI36
NG_032093.1:g.428068G>T
NG_032093.2:g.428068G>T
NG_066624.1:g.429972G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4613G>T	ENSP00000055163.8:p.Arg1538Leu
ENST00000414678.8:c.4682G>T	ENSP00000412835.3:p.Arg1561Leu
ENST00000637015.2:c.4901G>T	ENSP00000489729.2:p.Arg1634Leu
ENST00000346085.10:c.4652G>T	ENSP00000344546.5:p.Arg1551Leu
ENST00000350026.10:c.4364G>T	ENSP00000055163.7:p.Arg1455Leu
ENST00000414678.7:c.2930G>T	ENSP00000412835.2:p.Arg977Leu
ENST00000635849.1:c.2093G>T	ENSP00000490948.1:p.Arg698Leu
ENST00000635957.1:c.1724G>T	ENSP00000490385.1:p.Arg575Leu
ENST00000636227.1:n.3235G>T
ENST00000636254.1:n.692G>T
ENST00000636930.2:c.4772G>T MANE Select	ENSP00000490491.2:p.Arg1591Leu
ENST00000636940.1:n.2769G>T
ENST00000637015.1:c.2140G>T
ENST00000637568.1:c.2054G>T
ENST00000637741.1:n.1438G>T
ENST00000637810.1:c.2114G>T	ENSP00000489636.1:p.Arg705Leu
ENST00000637904.1:c.2273G>T	ENSP00000490550.1:p.Arg758Leu
ENST00000647938.1:c.4403G>T	ENSP00000498155.1:p.Arg1468Leu
ENST00000346085.9:c.4403G>T	ENSP00000344546.4:p.Arg1468Leu
ENST00000350026.9:c.4364G>T	ENSP00000055163.7:p.Arg1455Leu
ENST00000414678.6:c.2930G>T	ENSP00000412835.2:p.Arg977Leu
NM_017519.2:c.4364G>T	NP_059989.2:p.Arg1455Leu
NM_020732.3:c.4403G>T	NP_065783.3:p.Arg1468Leu
XM_005267069.3:c.4523G>T	XP_005267126.2:p.Arg1508Leu
XM_011535984.1:c.3602G>T	XP_011534286.1:p.Arg1201Leu
XM_011535985.1:c.3422G>T	XP_011534287.1:p.Arg1141Leu
XM_011535986.1:c.3182G>T	XP_011534288.1:p.Arg1061Leu
XM_011535987.1:c.2801G>T	XP_011534289.1:p.Arg934Leu
XM_011535988.1:c.1664G>T	XP_011534290.1:p.Arg555Leu
NM_001346813.1:c.4523G>T	NP_001333742.1:p.Arg1508Leu
NM_001363725.1:c.2273G>T	NP_001350654.1:p.Arg758Leu
XM_011535984.2:c.4733G>T	XP_011534286.2:p.Arg1578Leu
XM_011535988.3:c.1664G>T	XP_011534290.1:p.Arg555Leu
XM_017011103.2:c.4634G>T	XP_016866592.1:p.Arg1545Leu
XM_017011104.1:c.4604G>T	XP_016866593.1:p.Arg1535Leu
XM_017011105.2:c.4574G>T	XP_016866594.1:p.Arg1525Leu
XM_017011106.2:c.4445G>T	XP_016866595.1:p.Arg1482Leu
XM_017011107.2:c.4424G>T	XP_016866596.1:p.Arg1475Leu
XR_002956289.1:n.4719G>T
NM_001363725.2:c.2273G>T	NP_001350654.1:p.Arg758Leu
NM_001371656.1:c.4652G>T	NP_001358585.1:p.Arg1551Leu
NM_001374820.1:c.4652G>T	NP_001361749.1:p.Arg1551Leu
NM_001374828.1:c.4772G>T MANE Select	NP_001361757.1:p.Arg1591Leu
NM_017519.3:c.4613G>T	NP_059989.3:p.Arg1538Leu