Canonical Allele Identifier: CA366234622

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128339595
• MyVariant Identifiers: chr6:g.157511177G>C (hg19) ; chr6:g.157190043G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190043G>C , CM000668.2:g.157190043G>C	GRCh38
NC_000006.11:g.157511177G>C , CM000668.1:g.157511177G>C	GRCh37
NC_000006.10:g.157552869G>C	NCBI36
NG_032093.1:g.417114G>C
NG_032093.2:g.417114G>C
NG_066624.1:g.419018G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3905G>C	ENSP00000055163.8:p.Ser1302Thr
ENST00000414678.8:c.3974G>C	ENSP00000412835.3:p.Ser1325Thr
ENST00000637015.2:c.4193G>C	ENSP00000489729.2:p.Ser1398Thr
ENST00000346085.10:c.3944G>C	ENSP00000344546.5:p.Ser1315Thr
ENST00000350026.10:c.3656G>C	ENSP00000055163.7:p.Ser1219Thr
ENST00000414678.7:c.2222G>C	ENSP00000412835.2:p.Ser741Thr
ENST00000635849.1:c.1385G>C	ENSP00000490948.1:p.Ser462Thr
ENST00000635957.1:c.1016G>C	ENSP00000490385.1:p.Ser339Thr
ENST00000636930.2:c.4064G>C MANE Select	ENSP00000490491.2:p.Ser1355Thr
ENST00000636940.1:n.2061G>C
ENST00000637015.1:c.1432G>C
ENST00000637568.1:c.1346G>C
ENST00000637741.1:n.730G>C
ENST00000637810.1:c.1406G>C	ENSP00000489636.1:p.Ser469Thr
ENST00000637904.1:c.1565G>C	ENSP00000490550.1:p.Ser522Thr
ENST00000647938.1:c.3695G>C	ENSP00000498155.1:p.Ser1232Thr
ENST00000346085.9:c.3695G>C	ENSP00000344546.4:p.Ser1232Thr
ENST00000350026.9:c.3656G>C	ENSP00000055163.7:p.Ser1219Thr
ENST00000414678.6:c.2222G>C	ENSP00000412835.2:p.Ser741Thr
NM_017519.2:c.3656G>C	NP_059989.2:p.Ser1219Thr
NM_020732.3:c.3695G>C	NP_065783.3:p.Ser1232Thr
XM_005267069.3:c.3815G>C	XP_005267126.2:p.Ser1272Thr
XM_011535984.1:c.2894G>C	XP_011534286.1:p.Ser965Thr
XM_011535985.1:c.2714G>C	XP_011534287.1:p.Ser905Thr
XM_011535986.1:c.2474G>C	XP_011534288.1:p.Ser825Thr
XM_011535987.1:c.2093G>C	XP_011534289.1:p.Ser698Thr
XM_011535988.1:c.956G>C	XP_011534290.1:p.Ser319Thr
NM_001346813.1:c.3815G>C	NP_001333742.1:p.Ser1272Thr
NM_001363725.1:c.1565G>C	NP_001350654.1:p.Ser522Thr
XM_011535984.2:c.4025G>C	XP_011534286.2:p.Ser1342Thr
XM_011535988.3:c.956G>C	XP_011534290.1:p.Ser319Thr
XM_017011103.2:c.3926G>C	XP_016866592.1:p.Ser1309Thr
XM_017011104.1:c.3896G>C	XP_016866593.1:p.Ser1299Thr
XM_017011105.2:c.3866G>C	XP_016866594.1:p.Ser1289Thr
XM_017011106.2:c.3737G>C	XP_016866595.1:p.Ser1246Thr
XM_017011107.2:c.3716G>C	XP_016866596.1:p.Ser1239Thr
XR_002956289.1:n.4108G>C
NM_001363725.2:c.1565G>C	NP_001350654.1:p.Ser522Thr
NM_001371656.1:c.3944G>C	NP_001358585.1:p.Ser1315Thr
NM_001374820.1:c.3944G>C	NP_001361749.1:p.Ser1315Thr
NM_001374828.1:c.4064G>C MANE Select	NP_001361757.1:p.Ser1355Thr
NM_017519.3:c.3905G>C	NP_059989.3:p.Ser1302Thr