Canonical Allele Identifier: CA366241132

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157200877-G-T
• MyVariant Identifiers: chr6:g.157522011G>T (hg19) ; chr6:g.157200877G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200877G>T , CM000668.2:g.157200877G>T	GRCh38
NC_000006.11:g.157522011G>T , CM000668.1:g.157522011G>T	GRCh37
NC_000006.10:g.157563703G>T	NCBI36
NG_032093.1:g.427948G>T
NG_032093.2:g.427948G>T
NG_066624.1:g.429852G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4493G>T	ENSP00000055163.8:p.Ser1498Ile
ENST00000414678.8:c.4562G>T	ENSP00000412835.3:p.Ser1521Ile
ENST00000637015.2:c.4781G>T	ENSP00000489729.2:p.Ser1594Ile
ENST00000346085.10:c.4532G>T	ENSP00000344546.5:p.Ser1511Ile
ENST00000350026.10:c.4244G>T	ENSP00000055163.7:p.Ser1415Ile
ENST00000414678.7:c.2810G>T	ENSP00000412835.2:p.Ser937Ile
ENST00000635849.1:c.1973G>T	ENSP00000490948.1:p.Ser658Ile
ENST00000635957.1:c.1604G>T	ENSP00000490385.1:p.Ser535Ile
ENST00000636227.1:n.3115G>T
ENST00000636254.1:n.572G>T
ENST00000636930.2:c.4652G>T MANE Select	ENSP00000490491.2:p.Ser1551Ile
ENST00000636940.1:n.2649G>T
ENST00000637015.1:c.2020G>T
ENST00000637568.1:c.1934G>T
ENST00000637741.1:n.1318G>T
ENST00000637810.1:c.1994G>T	ENSP00000489636.1:p.Ser665Ile
ENST00000637904.1:c.2153G>T	ENSP00000490550.1:p.Ser718Ile
ENST00000647938.1:c.4283G>T	ENSP00000498155.1:p.Ser1428Ile
ENST00000346085.9:c.4283G>T	ENSP00000344546.4:p.Ser1428Ile
ENST00000350026.9:c.4244G>T	ENSP00000055163.7:p.Ser1415Ile
ENST00000414678.6:c.2810G>T	ENSP00000412835.2:p.Ser937Ile
NM_017519.2:c.4244G>T	NP_059989.2:p.Ser1415Ile
NM_020732.3:c.4283G>T	NP_065783.3:p.Ser1428Ile
XM_005267069.3:c.4403G>T	XP_005267126.2:p.Ser1468Ile
XM_011535984.1:c.3482G>T	XP_011534286.1:p.Ser1161Ile
XM_011535985.1:c.3302G>T	XP_011534287.1:p.Ser1101Ile
XM_011535986.1:c.3062G>T	XP_011534288.1:p.Ser1021Ile
XM_011535987.1:c.2681G>T	XP_011534289.1:p.Ser894Ile
XM_011535988.1:c.1544G>T	XP_011534290.1:p.Ser515Ile
NM_001346813.1:c.4403G>T	NP_001333742.1:p.Ser1468Ile
NM_001363725.1:c.2153G>T	NP_001350654.1:p.Ser718Ile
XM_011535984.2:c.4613G>T	XP_011534286.2:p.Ser1538Ile
XM_011535988.3:c.1544G>T	XP_011534290.1:p.Ser515Ile
XM_017011103.2:c.4514G>T	XP_016866592.1:p.Ser1505Ile
XM_017011104.1:c.4484G>T	XP_016866593.1:p.Ser1495Ile
XM_017011105.2:c.4454G>T	XP_016866594.1:p.Ser1485Ile
XM_017011106.2:c.4325G>T	XP_016866595.1:p.Ser1442Ile
XM_017011107.2:c.4304G>T	XP_016866596.1:p.Ser1435Ile
XR_002956289.1:n.4599G>T
NM_001363725.2:c.2153G>T	NP_001350654.1:p.Ser718Ile
NM_001371656.1:c.4532G>T	NP_001358585.1:p.Ser1511Ile
NM_001374820.1:c.4532G>T	NP_001361749.1:p.Ser1511Ile
NM_001374828.1:c.4652G>T MANE Select	NP_001361757.1:p.Ser1551Ile
NM_017519.3:c.4493G>T	NP_059989.3:p.Ser1498Ile