Canonical Allele Identifier: CA366240912

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157521913G>C (hg19) ; chr6:g.157200779G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200779G>C , CM000668.2:g.157200779G>C	GRCh38
NC_000006.11:g.157521913G>C , CM000668.1:g.157521913G>C	GRCh37
NC_000006.10:g.157563605G>C	NCBI36
NG_032093.1:g.427850G>C
NG_032093.2:g.427850G>C
NG_066624.1:g.429754G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4395G>C	ENSP00000055163.8:p.Gln1465His
ENST00000414678.8:c.4464G>C	ENSP00000412835.3:p.Gln1488His
ENST00000637015.2:c.4683G>C	ENSP00000489729.2:p.Gln1561His
ENST00000346085.10:c.4434G>C	ENSP00000344546.5:p.Gln1478His
ENST00000350026.10:c.4146G>C	ENSP00000055163.7:p.Gln1382His
ENST00000414678.7:c.2712G>C	ENSP00000412835.2:p.Gln904His
ENST00000635849.1:c.1875G>C	ENSP00000490948.1:p.Gln625His
ENST00000635957.1:c.1506G>C	ENSP00000490385.1:p.Gln502His
ENST00000636227.1:n.3017G>C
ENST00000636254.1:n.474G>C
ENST00000636930.2:c.4554G>C MANE Select	ENSP00000490491.2:p.Gln1518His
ENST00000636940.1:n.2551G>C
ENST00000637015.1:c.1922G>C
ENST00000637568.1:c.1836G>C
ENST00000637741.1:n.1220G>C
ENST00000637810.1:c.1896G>C	ENSP00000489636.1:p.Gln632His
ENST00000637904.1:c.2055G>C	ENSP00000490550.1:p.Gln685His
ENST00000647938.1:c.4185G>C	ENSP00000498155.1:p.Gln1395His
ENST00000346085.9:c.4185G>C	ENSP00000344546.4:p.Gln1395His
ENST00000350026.9:c.4146G>C	ENSP00000055163.7:p.Gln1382His
ENST00000414678.6:c.2712G>C	ENSP00000412835.2:p.Gln904His
NM_017519.2:c.4146G>C	NP_059989.2:p.Gln1382His
NM_020732.3:c.4185G>C	NP_065783.3:p.Gln1395His
XM_005267069.3:c.4305G>C	XP_005267126.2:p.Gln1435His
XM_011535984.1:c.3384G>C	XP_011534286.1:p.Gln1128His
XM_011535985.1:c.3204G>C	XP_011534287.1:p.Gln1068His
XM_011535986.1:c.2964G>C	XP_011534288.1:p.Gln988His
XM_011535987.1:c.2583G>C	XP_011534289.1:p.Gln861His
XM_011535988.1:c.1446G>C	XP_011534290.1:p.Gln482His
NM_001346813.1:c.4305G>C	NP_001333742.1:p.Gln1435His
NM_001363725.1:c.2055G>C	NP_001350654.1:p.Gln685His
XM_011535984.2:c.4515G>C	XP_011534286.2:p.Gln1505His
XM_011535988.3:c.1446G>C	XP_011534290.1:p.Gln482His
XM_017011103.2:c.4416G>C	XP_016866592.1:p.Gln1472His
XM_017011104.1:c.4386G>C	XP_016866593.1:p.Gln1462His
XM_017011105.2:c.4356G>C	XP_016866594.1:p.Gln1452His
XM_017011106.2:c.4227G>C	XP_016866595.1:p.Gln1409His
XM_017011107.2:c.4206G>C	XP_016866596.1:p.Gln1402His
XR_002956289.1:n.4501G>C
NM_001363725.2:c.2055G>C	NP_001350654.1:p.Gln685His
NM_001371656.1:c.4434G>C	NP_001358585.1:p.Gln1478His
NM_001374820.1:c.4434G>C	NP_001361749.1:p.Gln1478His
NM_001374828.1:c.4554G>C MANE Select	NP_001361757.1:p.Gln1518His
NM_017519.3:c.4395G>C	NP_059989.3:p.Gln1465His