Canonical Allele Identifier: CA366235281

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511240C>A (hg19) ; chr6:g.157190106C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190106C>A , CM000668.2:g.157190106C>A	GRCh38
NC_000006.11:g.157511240C>A , CM000668.1:g.157511240C>A	GRCh37
NC_000006.10:g.157552932C>A	NCBI36
NG_032093.1:g.417177C>A
NG_032093.2:g.417177C>A
NG_066624.1:g.419081C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3968C>A	ENSP00000055163.8:p.Ser1323Tyr
ENST00000414678.8:c.4037C>A	ENSP00000412835.3:p.Ser1346Tyr
ENST00000637015.2:c.4256C>A	ENSP00000489729.2:p.Ser1419Tyr
ENST00000346085.10:c.4007C>A	ENSP00000344546.5:p.Ser1336Tyr
ENST00000350026.10:c.3719C>A	ENSP00000055163.7:p.Ser1240Tyr
ENST00000414678.7:c.2285C>A	ENSP00000412835.2:p.Ser762Tyr
ENST00000635849.1:c.1448C>A	ENSP00000490948.1:p.Ser483Tyr
ENST00000635957.1:c.1079C>A	ENSP00000490385.1:p.Ser360Tyr
ENST00000636930.2:c.4127C>A MANE Select	ENSP00000490491.2:p.Ser1376Tyr
ENST00000636940.1:n.2124C>A
ENST00000637015.1:c.1495C>A
ENST00000637568.1:c.1409C>A
ENST00000637741.1:n.793C>A
ENST00000637810.1:c.1469C>A	ENSP00000489636.1:p.Ser490Tyr
ENST00000637904.1:c.1628C>A	ENSP00000490550.1:p.Ser543Tyr
ENST00000647938.1:c.3758C>A	ENSP00000498155.1:p.Ser1253Tyr
ENST00000346085.9:c.3758C>A	ENSP00000344546.4:p.Ser1253Tyr
ENST00000350026.9:c.3719C>A	ENSP00000055163.7:p.Ser1240Tyr
ENST00000414678.6:c.2285C>A	ENSP00000412835.2:p.Ser762Tyr
NM_017519.2:c.3719C>A	NP_059989.2:p.Ser1240Tyr
NM_020732.3:c.3758C>A	NP_065783.3:p.Ser1253Tyr
XM_005267069.3:c.3878C>A	XP_005267126.2:p.Ser1293Tyr
XM_011535984.1:c.2957C>A	XP_011534286.1:p.Ser986Tyr
XM_011535985.1:c.2777C>A	XP_011534287.1:p.Ser926Tyr
XM_011535986.1:c.2537C>A	XP_011534288.1:p.Ser846Tyr
XM_011535987.1:c.2156C>A	XP_011534289.1:p.Ser719Tyr
XM_011535988.1:c.1019C>A	XP_011534290.1:p.Ser340Tyr
NM_001346813.1:c.3878C>A	NP_001333742.1:p.Ser1293Tyr
NM_001363725.1:c.1628C>A	NP_001350654.1:p.Ser543Tyr
XM_011535984.2:c.4088C>A	XP_011534286.2:p.Ser1363Tyr
XM_011535988.3:c.1019C>A	XP_011534290.1:p.Ser340Tyr
XM_017011103.2:c.3989C>A	XP_016866592.1:p.Ser1330Tyr
XM_017011104.1:c.3959C>A	XP_016866593.1:p.Ser1320Tyr
XM_017011105.2:c.3929C>A	XP_016866594.1:p.Ser1310Tyr
XM_017011106.2:c.3800C>A	XP_016866595.1:p.Ser1267Tyr
XM_017011107.2:c.3779C>A	XP_016866596.1:p.Ser1260Tyr
XR_002956289.1:n.4171C>A
NM_001363725.2:c.1628C>A	NP_001350654.1:p.Ser543Tyr
NM_001371656.1:c.4007C>A	NP_001358585.1:p.Ser1336Tyr
NM_001374820.1:c.4007C>A	NP_001361749.1:p.Ser1336Tyr
NM_001374828.1:c.4127C>A MANE Select	NP_001361757.1:p.Ser1376Tyr
NM_017519.3:c.3968C>A	NP_059989.3:p.Ser1323Tyr