Canonical Allele Identifier: CA366235282

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3968C>G	ENSP00000055163.8:p.Ser1323Cys
ENST00000414678.8:c.4037C>G	ENSP00000412835.3:p.Ser1346Cys
ENST00000637015.2:c.4256C>G	ENSP00000489729.2:p.Ser1419Cys
ENST00000346085.10:c.4007C>G	ENSP00000344546.5:p.Ser1336Cys
ENST00000350026.10:c.3719C>G	ENSP00000055163.7:p.Ser1240Cys
ENST00000414678.7:c.2285C>G	ENSP00000412835.2:p.Ser762Cys
ENST00000635849.1:c.1448C>G	ENSP00000490948.1:p.Ser483Cys
ENST00000635957.1:c.1079C>G	ENSP00000490385.1:p.Ser360Cys
ENST00000636930.2:c.4127C>G MANE Select	ENSP00000490491.2:p.Ser1376Cys
ENST00000636940.1:n.2124C>G
ENST00000637015.1:c.1495C>G
ENST00000637568.1:c.1409C>G
ENST00000637741.1:n.793C>G
ENST00000637810.1:c.1469C>G	ENSP00000489636.1:p.Ser490Cys
ENST00000637904.1:c.1628C>G	ENSP00000490550.1:p.Ser543Cys
ENST00000647938.1:c.3758C>G	ENSP00000498155.1:p.Ser1253Cys
ENST00000346085.9:c.3758C>G	ENSP00000344546.4:p.Ser1253Cys
ENST00000350026.9:c.3719C>G	ENSP00000055163.7:p.Ser1240Cys
ENST00000414678.6:c.2285C>G	ENSP00000412835.2:p.Ser762Cys
NM_017519.2:c.3719C>G	NP_059989.2:p.Ser1240Cys
NM_020732.3:c.3758C>G	NP_065783.3:p.Ser1253Cys
XM_005267069.3:c.3878C>G	XP_005267126.2:p.Ser1293Cys
XM_011535984.1:c.2957C>G	XP_011534286.1:p.Ser986Cys
XM_011535985.1:c.2777C>G	XP_011534287.1:p.Ser926Cys
XM_011535986.1:c.2537C>G	XP_011534288.1:p.Ser846Cys
XM_011535987.1:c.2156C>G	XP_011534289.1:p.Ser719Cys
XM_011535988.1:c.1019C>G	XP_011534290.1:p.Ser340Cys
NM_001346813.1:c.3878C>G	NP_001333742.1:p.Ser1293Cys
NM_001363725.1:c.1628C>G	NP_001350654.1:p.Ser543Cys
XM_011535984.2:c.4088C>G	XP_011534286.2:p.Ser1363Cys
XM_011535988.3:c.1019C>G	XP_011534290.1:p.Ser340Cys
XM_017011103.2:c.3989C>G	XP_016866592.1:p.Ser1330Cys
XM_017011104.1:c.3959C>G	XP_016866593.1:p.Ser1320Cys
XM_017011105.2:c.3929C>G	XP_016866594.1:p.Ser1310Cys
XM_017011106.2:c.3800C>G	XP_016866595.1:p.Ser1267Cys
XM_017011107.2:c.3779C>G	XP_016866596.1:p.Ser1260Cys
XR_002956289.1:n.4171C>G
NM_001363725.2:c.1628C>G	NP_001350654.1:p.Ser543Cys
NM_001371656.1:c.4007C>G	NP_001358585.1:p.Ser1336Cys
NM_001374820.1:c.4007C>G	NP_001361749.1:p.Ser1336Cys
NM_001374828.1:c.4127C>G MANE Select	NP_001361757.1:p.Ser1376Cys
NM_017519.3:c.3968C>G	NP_059989.3:p.Ser1323Cys