Canonical Allele Identifier: CA366234935

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511203T>C (hg19) ; chr6:g.157190069T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190069T>C , CM000668.2:g.157190069T>C	GRCh38
NC_000006.11:g.157511203T>C , CM000668.1:g.157511203T>C	GRCh37
NC_000006.10:g.157552895T>C	NCBI36
NG_032093.1:g.417140T>C
NG_032093.2:g.417140T>C
NG_066624.1:g.419044T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3931T>C	ENSP00000055163.8:p.Ser1311Pro
ENST00000414678.8:c.4000T>C	ENSP00000412835.3:p.Ser1334Pro
ENST00000637015.2:c.4219T>C	ENSP00000489729.2:p.Ser1407Pro
ENST00000346085.10:c.3970T>C	ENSP00000344546.5:p.Ser1324Pro
ENST00000350026.10:c.3682T>C	ENSP00000055163.7:p.Ser1228Pro
ENST00000414678.7:c.2248T>C	ENSP00000412835.2:p.Ser750Pro
ENST00000635849.1:c.1411T>C	ENSP00000490948.1:p.Ser471Pro
ENST00000635957.1:c.1042T>C	ENSP00000490385.1:p.Ser348Pro
ENST00000636930.2:c.4090T>C MANE Select	ENSP00000490491.2:p.Ser1364Pro
ENST00000636940.1:n.2087T>C
ENST00000637015.1:c.1458T>C
ENST00000637568.1:c.1372T>C
ENST00000637741.1:n.756T>C
ENST00000637810.1:c.1432T>C	ENSP00000489636.1:p.Ser478Pro
ENST00000637904.1:c.1591T>C	ENSP00000490550.1:p.Ser531Pro
ENST00000647938.1:c.3721T>C	ENSP00000498155.1:p.Ser1241Pro
ENST00000346085.9:c.3721T>C	ENSP00000344546.4:p.Ser1241Pro
ENST00000350026.9:c.3682T>C	ENSP00000055163.7:p.Ser1228Pro
ENST00000414678.6:c.2248T>C	ENSP00000412835.2:p.Ser750Pro
NM_017519.2:c.3682T>C	NP_059989.2:p.Ser1228Pro
NM_020732.3:c.3721T>C	NP_065783.3:p.Ser1241Pro
XM_005267069.3:c.3841T>C	XP_005267126.2:p.Ser1281Pro
XM_011535984.1:c.2920T>C	XP_011534286.1:p.Ser974Pro
XM_011535985.1:c.2740T>C	XP_011534287.1:p.Ser914Pro
XM_011535986.1:c.2500T>C	XP_011534288.1:p.Ser834Pro
XM_011535987.1:c.2119T>C	XP_011534289.1:p.Ser707Pro
XM_011535988.1:c.982T>C	XP_011534290.1:p.Ser328Pro
NM_001346813.1:c.3841T>C	NP_001333742.1:p.Ser1281Pro
NM_001363725.1:c.1591T>C	NP_001350654.1:p.Ser531Pro
XM_011535984.2:c.4051T>C	XP_011534286.2:p.Ser1351Pro
XM_011535988.3:c.982T>C	XP_011534290.1:p.Ser328Pro
XM_017011103.2:c.3952T>C	XP_016866592.1:p.Ser1318Pro
XM_017011104.1:c.3922T>C	XP_016866593.1:p.Ser1308Pro
XM_017011105.2:c.3892T>C	XP_016866594.1:p.Ser1298Pro
XM_017011106.2:c.3763T>C	XP_016866595.1:p.Ser1255Pro
XM_017011107.2:c.3742T>C	XP_016866596.1:p.Ser1248Pro
XR_002956289.1:n.4134T>C
NM_001363725.2:c.1591T>C	NP_001350654.1:p.Ser531Pro
NM_001371656.1:c.3970T>C	NP_001358585.1:p.Ser1324Pro
NM_001374820.1:c.3970T>C	NP_001361749.1:p.Ser1324Pro
NM_001374828.1:c.4090T>C MANE Select	NP_001361757.1:p.Ser1364Pro
NM_017519.3:c.3931T>C	NP_059989.3:p.Ser1311Pro