Canonical Allele Identifier: CA366234160

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510854T>A (hg19) ; chr6:g.157189720T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189720T>A , CM000668.2:g.157189720T>A	GRCh38
NC_000006.11:g.157510854T>A , CM000668.1:g.157510854T>A	GRCh37
NC_000006.10:g.157552546T>A	NCBI36
NG_032093.1:g.416791T>A
NG_032093.2:g.416791T>A
NG_066624.1:g.418695T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3839T>A	ENSP00000055163.8:p.Leu1280Gln
ENST00000414678.8:c.3908T>A	ENSP00000412835.3:p.Leu1303Gln
ENST00000637015.2:c.4127T>A	ENSP00000489729.2:p.Leu1376Gln
ENST00000346085.10:c.3878T>A	ENSP00000344546.5:p.Leu1293Gln
ENST00000350026.10:c.3590T>A	ENSP00000055163.7:p.Leu1197Gln
ENST00000414678.7:c.2156T>A	ENSP00000412835.2:p.Leu719Gln
ENST00000635849.1:c.1319T>A	ENSP00000490948.1:p.Leu440Gln
ENST00000635957.1:c.953T>A	ENSP00000490385.1:p.Leu318Gln
ENST00000636930.2:c.3998T>A MANE Select	ENSP00000490491.2:p.Leu1333Gln
ENST00000636940.1:n.1995T>A
ENST00000637015.1:c.1366T>A
ENST00000637568.1:c.1280T>A
ENST00000637741.1:n.664T>A
ENST00000637810.1:c.1340T>A	ENSP00000489636.1:p.Leu447Gln
ENST00000637904.1:c.1499T>A	ENSP00000490550.1:p.Leu500Gln
ENST00000647938.1:c.3629T>A	ENSP00000498155.1:p.Leu1210Gln
ENST00000346085.9:c.3629T>A	ENSP00000344546.4:p.Leu1210Gln
ENST00000350026.9:c.3590T>A	ENSP00000055163.7:p.Leu1197Gln
ENST00000414678.6:c.2156T>A	ENSP00000412835.2:p.Leu719Gln
NM_017519.2:c.3590T>A	NP_059989.2:p.Leu1197Gln
NM_020732.3:c.3629T>A	NP_065783.3:p.Leu1210Gln
XM_005267069.3:c.3749T>A	XP_005267126.2:p.Leu1250Gln
XM_011535984.1:c.2828T>A	XP_011534286.1:p.Leu943Gln
XM_011535985.1:c.2648T>A	XP_011534287.1:p.Leu883Gln
XM_011535986.1:c.2408T>A	XP_011534288.1:p.Leu803Gln
XM_011535987.1:c.2027T>A	XP_011534289.1:p.Leu676Gln
XM_011535988.1:c.890T>A	XP_011534290.1:p.Leu297Gln
NM_001346813.1:c.3749T>A	NP_001333742.1:p.Leu1250Gln
NM_001363725.1:c.1499T>A	NP_001350654.1:p.Leu500Gln
XM_011535984.2:c.3959T>A	XP_011534286.2:p.Leu1320Gln
XM_011535988.3:c.890T>A	XP_011534290.1:p.Leu297Gln
XM_017011103.2:c.3860T>A	XP_016866592.1:p.Leu1287Gln
XM_017011104.1:c.3830T>A	XP_016866593.1:p.Leu1277Gln
XM_017011105.2:c.3800T>A	XP_016866594.1:p.Leu1267Gln
XM_017011106.2:c.3671T>A	XP_016866595.1:p.Leu1224Gln
XM_017011107.2:c.3650T>A	XP_016866596.1:p.Leu1217Gln
XR_002956289.1:n.4042T>A
NM_001363725.2:c.1499T>A	NP_001350654.1:p.Leu500Gln
NM_001371656.1:c.3878T>A	NP_001358585.1:p.Leu1293Gln
NM_001374820.1:c.3878T>A	NP_001361749.1:p.Leu1293Gln
NM_001374828.1:c.3998T>A MANE Select	NP_001361757.1:p.Leu1333Gln
NM_017519.3:c.3839T>A	NP_059989.3:p.Leu1280Gln