Canonical Allele Identifier: CA4067698

Gene: ARID1B

Linked Data

• dbSNP Id: rs756120841
• ExAC: 6:157522096 C / T
• gnomAD v2: 6-157522096-C-T
• gnomAD v4: 6-157200962-C-T
• MyVariant Identifiers: chr6:g.157522096C>T (hg19) ; chr6:g.157200962C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200962C>T , CM000668.2:g.157200962C>T	GRCh38
NC_000006.11:g.157522096C>T , CM000668.1:g.157522096C>T	GRCh37
NC_000006.10:g.157563788C>T	NCBI36
NG_032093.1:g.428033C>T
NG_032093.2:g.428033C>T
NG_066624.1:g.429937C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.4578C>T	ENSP00000055163.8:p.Ser1526=
ENST00000414678.8:c.4647C>T	ENSP00000412835.3:p.Ser1549=
ENST00000637015.2:c.4866C>T	ENSP00000489729.2:p.Ser1622=
ENST00000346085.10:c.4617C>T	ENSP00000344546.5:p.Ser1539=
ENST00000350026.10:c.4329C>T	ENSP00000055163.7:p.Ser1443=
ENST00000414678.7:c.2895C>T	ENSP00000412835.2:p.Ser965=
ENST00000635849.1:c.2058C>T	ENSP00000490948.1:p.Ser686=
ENST00000635957.1:c.1689C>T	ENSP00000490385.1:p.Ser563=
ENST00000636227.1:n.3200C>T
ENST00000636254.1:n.657C>T
ENST00000636930.2:c.4737C>T MANE Select	ENSP00000490491.2:p.Ser1579=
ENST00000636940.1:n.2734C>T
ENST00000637015.1:c.2105C>T
ENST00000637568.1:c.2019C>T
ENST00000637741.1:n.1403C>T
ENST00000637810.1:c.2079C>T	ENSP00000489636.1:p.Ser693=
ENST00000637904.1:c.2238C>T	ENSP00000490550.1:p.Ser746=
ENST00000647938.1:c.4368C>T	ENSP00000498155.1:p.Ser1456=
ENST00000346085.9:c.4368C>T	ENSP00000344546.4:p.Ser1456=
ENST00000350026.9:c.4329C>T	ENSP00000055163.7:p.Ser1443=
ENST00000414678.6:c.2895C>T	ENSP00000412835.2:p.Ser965=
NM_017519.2:c.4329C>T	NP_059989.2:p.Ser1443=
NM_020732.3:c.4368C>T	NP_065783.3:p.Ser1456=
XM_005267069.3:c.4488C>T	XP_005267126.2:p.Ser1496=
XM_011535984.1:c.3567C>T	XP_011534286.1:p.Ser1189=
XM_011535985.1:c.3387C>T	XP_011534287.1:p.Ser1129=
XM_011535986.1:c.3147C>T	XP_011534288.1:p.Ser1049=
XM_011535987.1:c.2766C>T	XP_011534289.1:p.Ser922=
XM_011535988.1:c.1629C>T	XP_011534290.1:p.Ser543=
NM_001346813.1:c.4488C>T	NP_001333742.1:p.Ser1496=
NM_001363725.1:c.2238C>T	NP_001350654.1:p.Ser746=
XM_011535984.2:c.4698C>T	XP_011534286.2:p.Ser1566=
XM_011535988.3:c.1629C>T	XP_011534290.1:p.Ser543=
XM_017011103.2:c.4599C>T	XP_016866592.1:p.Ser1533=
XM_017011104.1:c.4569C>T	XP_016866593.1:p.Ser1523=
XM_017011105.2:c.4539C>T	XP_016866594.1:p.Ser1513=
XM_017011106.2:c.4410C>T	XP_016866595.1:p.Ser1470=
XM_017011107.2:c.4389C>T	XP_016866596.1:p.Ser1463=
XR_002956289.1:n.4684C>T
NM_001363725.2:c.2238C>T	NP_001350654.1:p.Ser746=
NM_001371656.1:c.4617C>T	NP_001358585.1:p.Ser1539=
NM_001374820.1:c.4617C>T	NP_001361749.1:p.Ser1539=
NM_001374828.1:c.4737C>T MANE Select	NP_001361757.1:p.Ser1579=
NM_017519.3:c.4578C>T	NP_059989.3:p.Ser1526=