Canonical Allele Identifier: CA366242396

Gene: ARID1B

Linked Data

• dbSNP Id: rs1312924715
• gnomAD v3: 6-157201281-C-A
• gnomAD v4: 6-157201281-C-A
• MyVariant Identifiers: chr6:g.157522415C>A (hg19) ; chr6:g.157201281C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201281C>A , CM000668.2:g.157201281C>A	GRCh38
NC_000006.11:g.157522415C>A , CM000668.1:g.157522415C>A	GRCh37
NC_000006.10:g.157564107C>A	NCBI36
NG_032093.1:g.428352C>A
NG_032093.2:g.428352C>A
NG_066624.1:g.430256C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4897C>A	ENSP00000055163.8:p.Leu1633Met
ENST00000414678.8:c.4966C>A	ENSP00000412835.3:p.Leu1656Met
ENST00000637015.2:c.5185C>A	ENSP00000489729.2:p.Leu1729Met
ENST00000346085.10:c.4936C>A	ENSP00000344546.5:p.Leu1646Met
ENST00000350026.10:c.4648C>A	ENSP00000055163.7:p.Leu1550Met
ENST00000414678.7:c.3214C>A	ENSP00000412835.2:p.Leu1072Met
ENST00000635849.1:c.2377C>A	ENSP00000490948.1:p.Leu793Met
ENST00000635957.1:c.2008C>A	ENSP00000490385.1:p.Leu670Met
ENST00000636227.1:n.3519C>A
ENST00000636254.1:n.976C>A
ENST00000636930.2:c.5056C>A MANE Select	ENSP00000490491.2:p.Leu1686Met
ENST00000636940.1:n.3053C>A
ENST00000637015.1:c.2424C>A
ENST00000637568.1:c.2338C>A
ENST00000637741.1:n.1722C>A
ENST00000637810.1:c.2398C>A	ENSP00000489636.1:p.Leu800Met
ENST00000637904.1:c.2557C>A	ENSP00000490550.1:p.Leu853Met
ENST00000647938.1:c.4687C>A	ENSP00000498155.1:p.Leu1563Met
ENST00000346085.9:c.4687C>A	ENSP00000344546.4:p.Leu1563Met
ENST00000350026.9:c.4648C>A	ENSP00000055163.7:p.Leu1550Met
ENST00000414678.6:c.3214C>A	ENSP00000412835.2:p.Leu1072Met
NM_017519.2:c.4648C>A	NP_059989.2:p.Leu1550Met
NM_020732.3:c.4687C>A	NP_065783.3:p.Leu1563Met
XM_005267069.3:c.4807C>A	XP_005267126.2:p.Leu1603Met
XM_011535984.1:c.3886C>A	XP_011534286.1:p.Leu1296Met
XM_011535985.1:c.3706C>A	XP_011534287.1:p.Leu1236Met
XM_011535986.1:c.3466C>A	XP_011534288.1:p.Leu1156Met
XM_011535987.1:c.3085C>A	XP_011534289.1:p.Leu1029Met
XM_011535988.1:c.1948C>A	XP_011534290.1:p.Leu650Met
NM_001346813.1:c.4807C>A	NP_001333742.1:p.Leu1603Met
NM_001363725.1:c.2557C>A	NP_001350654.1:p.Leu853Met
XM_011535984.2:c.5017C>A	XP_011534286.2:p.Leu1673Met
XM_011535988.3:c.1948C>A	XP_011534290.1:p.Leu650Met
XM_017011103.2:c.4918C>A	XP_016866592.1:p.Leu1640Met
XM_017011104.1:c.4888C>A	XP_016866593.1:p.Leu1630Met
XM_017011105.2:c.4858C>A	XP_016866594.1:p.Leu1620Met
XM_017011106.2:c.4729C>A	XP_016866595.1:p.Leu1577Met
XM_017011107.2:c.4708C>A	XP_016866596.1:p.Leu1570Met
XR_002956289.1:n.5003C>A
NM_001363725.2:c.2557C>A	NP_001350654.1:p.Leu853Met
NM_001371656.1:c.4936C>A	NP_001358585.1:p.Leu1646Met
NM_001374820.1:c.4936C>A	NP_001361749.1:p.Leu1646Met
NM_001374828.1:c.5056C>A MANE Select	NP_001361757.1:p.Leu1686Met
NM_017519.3:c.4897C>A	NP_059989.3:p.Leu1633Met