Canonical Allele Identifier: CA366235276

Gene: ARID1B

Linked Data

• dbSNP Id: rs1793249519
• gnomAD v3: 6-157190105-T-A
• gnomAD v4: 6-157190105-T-A
• MyVariant Identifiers: chr6:g.157511239T>A (hg19) ; chr6:g.157190105T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3967T>A	ENSP00000055163.8:p.Ser1323Thr
ENST00000414678.8:c.4036T>A	ENSP00000412835.3:p.Ser1346Thr
ENST00000637015.2:c.4255T>A	ENSP00000489729.2:p.Ser1419Thr
ENST00000346085.10:c.4006T>A	ENSP00000344546.5:p.Ser1336Thr
ENST00000350026.10:c.3718T>A	ENSP00000055163.7:p.Ser1240Thr
ENST00000414678.7:c.2284T>A	ENSP00000412835.2:p.Ser762Thr
ENST00000635849.1:c.1447T>A	ENSP00000490948.1:p.Ser483Thr
ENST00000635957.1:c.1078T>A	ENSP00000490385.1:p.Ser360Thr
ENST00000636930.2:c.4126T>A MANE Select	ENSP00000490491.2:p.Ser1376Thr
ENST00000636940.1:n.2123T>A
ENST00000637015.1:c.1494T>A
ENST00000637568.1:c.1408T>A
ENST00000637741.1:n.792T>A
ENST00000637810.1:c.1468T>A	ENSP00000489636.1:p.Ser490Thr
ENST00000637904.1:c.1627T>A	ENSP00000490550.1:p.Ser543Thr
ENST00000647938.1:c.3757T>A	ENSP00000498155.1:p.Ser1253Thr
ENST00000346085.9:c.3757T>A	ENSP00000344546.4:p.Ser1253Thr
ENST00000350026.9:c.3718T>A	ENSP00000055163.7:p.Ser1240Thr
ENST00000414678.6:c.2284T>A	ENSP00000412835.2:p.Ser762Thr
NM_017519.2:c.3718T>A	NP_059989.2:p.Ser1240Thr
NM_020732.3:c.3757T>A	NP_065783.3:p.Ser1253Thr
XM_005267069.3:c.3877T>A	XP_005267126.2:p.Ser1293Thr
XM_011535984.1:c.2956T>A	XP_011534286.1:p.Ser986Thr
XM_011535985.1:c.2776T>A	XP_011534287.1:p.Ser926Thr
XM_011535986.1:c.2536T>A	XP_011534288.1:p.Ser846Thr
XM_011535987.1:c.2155T>A	XP_011534289.1:p.Ser719Thr
XM_011535988.1:c.1018T>A	XP_011534290.1:p.Ser340Thr
NM_001346813.1:c.3877T>A	NP_001333742.1:p.Ser1293Thr
NM_001363725.1:c.1627T>A	NP_001350654.1:p.Ser543Thr
XM_011535984.2:c.4087T>A	XP_011534286.2:p.Ser1363Thr
XM_011535988.3:c.1018T>A	XP_011534290.1:p.Ser340Thr
XM_017011103.2:c.3988T>A	XP_016866592.1:p.Ser1330Thr
XM_017011104.1:c.3958T>A	XP_016866593.1:p.Ser1320Thr
XM_017011105.2:c.3928T>A	XP_016866594.1:p.Ser1310Thr
XM_017011106.2:c.3799T>A	XP_016866595.1:p.Ser1267Thr
XM_017011107.2:c.3778T>A	XP_016866596.1:p.Ser1260Thr
XR_002956289.1:n.4170T>A
NM_001363725.2:c.1627T>A	NP_001350654.1:p.Ser543Thr
NM_001371656.1:c.4006T>A	NP_001358585.1:p.Ser1336Thr
NM_001374820.1:c.4006T>A	NP_001361749.1:p.Ser1336Thr
NM_001374828.1:c.4126T>A MANE Select	NP_001361757.1:p.Ser1376Thr
NM_017519.3:c.3967T>A	NP_059989.3:p.Ser1323Thr