Canonical Allele Identifier: CA366239820

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366519
• MyVariant Identifiers: chr6:g.157520017G>C (hg19) ; chr6:g.157198883G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198883G>C , CM000668.2:g.157198883G>C	GRCh38
NC_000006.11:g.157520017G>C , CM000668.1:g.157520017G>C	GRCh37
NC_000006.10:g.157561709G>C	NCBI36
NG_032093.1:g.425954G>C
NG_032093.2:g.425954G>C
NG_066624.1:g.427858G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4296G>C	ENSP00000055163.8:p.Gln1432His
ENST00000414678.8:c.4365G>C	ENSP00000412835.3:p.Gln1455His
ENST00000637015.2:c.4584G>C	ENSP00000489729.2:p.Gln1528His
ENST00000346085.10:c.4335G>C	ENSP00000344546.5:p.Gln1445His
ENST00000350026.10:c.4047G>C	ENSP00000055163.7:p.Gln1349His
ENST00000414678.7:c.2613G>C	ENSP00000412835.2:p.Gln871His
ENST00000635849.1:c.1776G>C	ENSP00000490948.1:p.Gln592His
ENST00000635957.1:c.1407G>C	ENSP00000490385.1:p.Gln469His
ENST00000636227.1:n.2918G>C
ENST00000636254.1:n.375G>C
ENST00000636930.2:c.4455G>C MANE Select	ENSP00000490491.2:p.Gln1485His
ENST00000636940.1:n.2452G>C
ENST00000637015.1:c.1823G>C
ENST00000637568.1:c.1737G>C
ENST00000637741.1:n.1121G>C
ENST00000637810.1:c.1797G>C	ENSP00000489636.1:p.Gln599His
ENST00000637904.1:c.1956G>C	ENSP00000490550.1:p.Gln652His
ENST00000647938.1:c.4086G>C	ENSP00000498155.1:p.Gln1362His
ENST00000346085.9:c.4086G>C	ENSP00000344546.4:p.Gln1362His
ENST00000350026.9:c.4047G>C	ENSP00000055163.7:p.Gln1349His
ENST00000414678.6:c.2613G>C	ENSP00000412835.2:p.Gln871His
NM_017519.2:c.4047G>C	NP_059989.2:p.Gln1349His
NM_020732.3:c.4086G>C	NP_065783.3:p.Gln1362His
XM_005267069.3:c.4206G>C	XP_005267126.2:p.Gln1402His
XM_011535984.1:c.3285G>C	XP_011534286.1:p.Gln1095His
XM_011535985.1:c.3105G>C	XP_011534287.1:p.Gln1035His
XM_011535986.1:c.2865G>C	XP_011534288.1:p.Gln955His
XM_011535987.1:c.2484G>C	XP_011534289.1:p.Gln828His
XM_011535988.1:c.1347G>C	XP_011534290.1:p.Gln449His
NM_001346813.1:c.4206G>C	NP_001333742.1:p.Gln1402His
NM_001363725.1:c.1956G>C	NP_001350654.1:p.Gln652His
XM_011535984.2:c.4416G>C	XP_011534286.2:p.Gln1472His
XM_011535988.3:c.1347G>C	XP_011534290.1:p.Gln449His
XM_017011103.2:c.4317G>C	XP_016866592.1:p.Gln1439His
XM_017011104.1:c.4287G>C	XP_016866593.1:p.Gln1429His
XM_017011105.2:c.4257G>C	XP_016866594.1:p.Gln1419His
XM_017011106.2:c.4128G>C	XP_016866595.1:p.Gln1376His
XM_017011107.2:c.4107G>C	XP_016866596.1:p.Gln1369His
XR_002956289.1:n.4427-1822G>C
NM_001363725.2:c.1956G>C	NP_001350654.1:p.Gln652His
NM_001371656.1:c.4335G>C	NP_001358585.1:p.Gln1445His
NM_001374820.1:c.4335G>C	NP_001361749.1:p.Gln1445His
NM_001374828.1:c.4455G>C MANE Select	NP_001361757.1:p.Gln1485His
NM_017519.3:c.4296G>C	NP_059989.3:p.Gln1432His