Canonical Allele Identifier: CA452781584

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128339598
• MyVariant Identifiers: chr6:g.157511178T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190044T>C , CM000668.2:g.157190044T>C	GRCh38
NC_000006.11:g.157511178T>C , CM000668.1:g.157511178T>C	GRCh37
NC_000006.10:g.157552870T>C	NCBI36
NG_032093.1:g.417115T>C
NG_032093.2:g.417115T>C
NG_066624.1:g.419019T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3906T>C	ENSP00000055163.8:p.Ser1302=
ENST00000414678.8:c.3975T>C	ENSP00000412835.3:p.Ser1325=
ENST00000637015.2:c.4194T>C	ENSP00000489729.2:p.Ser1398=
ENST00000346085.10:c.3945T>C	ENSP00000344546.5:p.Ser1315=
ENST00000350026.10:c.3657T>C	ENSP00000055163.7:p.Ser1219=
ENST00000414678.7:c.2223T>C	ENSP00000412835.2:p.Ser741=
ENST00000635849.1:c.1386T>C	ENSP00000490948.1:p.Ser462=
ENST00000635957.1:c.1017T>C	ENSP00000490385.1:p.Ser339=
ENST00000636930.2:c.4065T>C MANE Select	ENSP00000490491.2:p.Ser1355=
ENST00000636940.1:n.2062T>C
ENST00000637015.1:c.1433T>C
ENST00000637568.1:c.1347T>C
ENST00000637741.1:n.731T>C
ENST00000637810.1:c.1407T>C	ENSP00000489636.1:p.Ser469=
ENST00000637904.1:c.1566T>C	ENSP00000490550.1:p.Ser522=
ENST00000647938.1:c.3696T>C	ENSP00000498155.1:p.Ser1232=
ENST00000346085.9:c.3696T>C	ENSP00000344546.4:p.Ser1232=
ENST00000350026.9:c.3657T>C	ENSP00000055163.7:p.Ser1219=
ENST00000414678.6:c.2223T>C	ENSP00000412835.2:p.Ser741=
NM_017519.2:c.3657T>C	NP_059989.2:p.Ser1219=
NM_020732.3:c.3696T>C	NP_065783.3:p.Ser1232=
XM_005267069.3:c.3816T>C	XP_005267126.2:p.Ser1272=
XM_011535984.1:c.2895T>C	XP_011534286.1:p.Ser965=
XM_011535985.1:c.2715T>C	XP_011534287.1:p.Ser905=
XM_011535986.1:c.2475T>C	XP_011534288.1:p.Ser825=
XM_011535987.1:c.2094T>C	XP_011534289.1:p.Ser698=
XM_011535988.1:c.957T>C	XP_011534290.1:p.Ser319=
NM_001346813.1:c.3816T>C	NP_001333742.1:p.Ser1272=
NM_001363725.1:c.1566T>C	NP_001350654.1:p.Ser522=
XM_011535984.2:c.4026T>C	XP_011534286.2:p.Ser1342=
XM_011535988.3:c.957T>C	XP_011534290.1:p.Ser319=
XM_017011103.2:c.3927T>C	XP_016866592.1:p.Ser1309=
XM_017011104.1:c.3897T>C	XP_016866593.1:p.Ser1299=
XM_017011105.2:c.3867T>C	XP_016866594.1:p.Ser1289=
XM_017011106.2:c.3738T>C	XP_016866595.1:p.Ser1246=
XM_017011107.2:c.3717T>C	XP_016866596.1:p.Ser1239=
XR_002956289.1:n.4109T>C
NM_001363725.2:c.1566T>C	NP_001350654.1:p.Ser522=
NM_001371656.1:c.3945T>C	NP_001358585.1:p.Ser1315=
NM_001374820.1:c.3945T>C	NP_001361749.1:p.Ser1315=
NM_001374828.1:c.4065T>C MANE Select	NP_001361757.1:p.Ser1355=
NM_017519.3:c.3906T>C	NP_059989.3:p.Ser1302=