Canonical Allele Identifier: CA366235279

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511239T>G (hg19) ; chr6:g.157190105T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190105T>G , CM000668.2:g.157190105T>G	GRCh38
NC_000006.11:g.157511239T>G , CM000668.1:g.157511239T>G	GRCh37
NC_000006.10:g.157552931T>G	NCBI36
NG_032093.1:g.417176T>G
NG_032093.2:g.417176T>G
NG_066624.1:g.419080T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3967T>G	ENSP00000055163.8:p.Ser1323Ala
ENST00000414678.8:c.4036T>G	ENSP00000412835.3:p.Ser1346Ala
ENST00000637015.2:c.4255T>G	ENSP00000489729.2:p.Ser1419Ala
ENST00000346085.10:c.4006T>G	ENSP00000344546.5:p.Ser1336Ala
ENST00000350026.10:c.3718T>G	ENSP00000055163.7:p.Ser1240Ala
ENST00000414678.7:c.2284T>G	ENSP00000412835.2:p.Ser762Ala
ENST00000635849.1:c.1447T>G	ENSP00000490948.1:p.Ser483Ala
ENST00000635957.1:c.1078T>G	ENSP00000490385.1:p.Ser360Ala
ENST00000636930.2:c.4126T>G MANE Select	ENSP00000490491.2:p.Ser1376Ala
ENST00000636940.1:n.2123T>G
ENST00000637015.1:c.1494T>G
ENST00000637568.1:c.1408T>G
ENST00000637741.1:n.792T>G
ENST00000637810.1:c.1468T>G	ENSP00000489636.1:p.Ser490Ala
ENST00000637904.1:c.1627T>G	ENSP00000490550.1:p.Ser543Ala
ENST00000647938.1:c.3757T>G	ENSP00000498155.1:p.Ser1253Ala
ENST00000346085.9:c.3757T>G	ENSP00000344546.4:p.Ser1253Ala
ENST00000350026.9:c.3718T>G	ENSP00000055163.7:p.Ser1240Ala
ENST00000414678.6:c.2284T>G	ENSP00000412835.2:p.Ser762Ala
NM_017519.2:c.3718T>G	NP_059989.2:p.Ser1240Ala
NM_020732.3:c.3757T>G	NP_065783.3:p.Ser1253Ala
XM_005267069.3:c.3877T>G	XP_005267126.2:p.Ser1293Ala
XM_011535984.1:c.2956T>G	XP_011534286.1:p.Ser986Ala
XM_011535985.1:c.2776T>G	XP_011534287.1:p.Ser926Ala
XM_011535986.1:c.2536T>G	XP_011534288.1:p.Ser846Ala
XM_011535987.1:c.2155T>G	XP_011534289.1:p.Ser719Ala
XM_011535988.1:c.1018T>G	XP_011534290.1:p.Ser340Ala
NM_001346813.1:c.3877T>G	NP_001333742.1:p.Ser1293Ala
NM_001363725.1:c.1627T>G	NP_001350654.1:p.Ser543Ala
XM_011535984.2:c.4087T>G	XP_011534286.2:p.Ser1363Ala
XM_011535988.3:c.1018T>G	XP_011534290.1:p.Ser340Ala
XM_017011103.2:c.3988T>G	XP_016866592.1:p.Ser1330Ala
XM_017011104.1:c.3958T>G	XP_016866593.1:p.Ser1320Ala
XM_017011105.2:c.3928T>G	XP_016866594.1:p.Ser1310Ala
XM_017011106.2:c.3799T>G	XP_016866595.1:p.Ser1267Ala
XM_017011107.2:c.3778T>G	XP_016866596.1:p.Ser1260Ala
XR_002956289.1:n.4170T>G
NM_001363725.2:c.1627T>G	NP_001350654.1:p.Ser543Ala
NM_001371656.1:c.4006T>G	NP_001358585.1:p.Ser1336Ala
NM_001374820.1:c.4006T>G	NP_001361749.1:p.Ser1336Ala
NM_001374828.1:c.4126T>G MANE Select	NP_001361757.1:p.Ser1376Ala
NM_017519.3:c.3967T>G	NP_059989.3:p.Ser1323Ala