Canonical Allele Identifier: CA366242503

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522451C>A (hg19) ; chr6:g.157201317C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201317C>A , CM000668.2:g.157201317C>A	GRCh38
NC_000006.11:g.157522451C>A , CM000668.1:g.157522451C>A	GRCh37
NC_000006.10:g.157564143C>A	NCBI36
NG_032093.1:g.428388C>A
NG_032093.2:g.428388C>A
NG_066624.1:g.430292C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4933C>A	ENSP00000055163.8:p.Leu1645Met
ENST00000414678.8:c.5002C>A	ENSP00000412835.3:p.Leu1668Met
ENST00000637015.2:c.5221C>A	ENSP00000489729.2:p.Leu1741Met
ENST00000346085.10:c.4972C>A	ENSP00000344546.5:p.Leu1658Met
ENST00000350026.10:c.4684C>A	ENSP00000055163.7:p.Leu1562Met
ENST00000414678.7:c.3250C>A	ENSP00000412835.2:p.Leu1084Met
ENST00000635849.1:c.2413C>A	ENSP00000490948.1:p.Leu805Met
ENST00000635957.1:c.2044C>A	ENSP00000490385.1:p.Leu682Met
ENST00000636227.1:n.3555C>A
ENST00000636254.1:n.1012C>A
ENST00000636930.2:c.5092C>A MANE Select	ENSP00000490491.2:p.Leu1698Met
ENST00000636940.1:n.3089C>A
ENST00000637015.1:c.2460C>A
ENST00000637568.1:c.2374C>A
ENST00000637741.1:n.1758C>A
ENST00000637810.1:c.2434C>A	ENSP00000489636.1:p.Leu812Met
ENST00000637904.1:c.2593C>A	ENSP00000490550.1:p.Leu865Met
ENST00000647938.1:c.4723C>A	ENSP00000498155.1:p.Leu1575Met
ENST00000346085.9:c.4723C>A	ENSP00000344546.4:p.Leu1575Met
ENST00000350026.9:c.4684C>A	ENSP00000055163.7:p.Leu1562Met
ENST00000414678.6:c.3250C>A	ENSP00000412835.2:p.Leu1084Met
NM_017519.2:c.4684C>A	NP_059989.2:p.Leu1562Met
NM_020732.3:c.4723C>A	NP_065783.3:p.Leu1575Met
XM_005267069.3:c.4843C>A	XP_005267126.2:p.Leu1615Met
XM_011535984.1:c.3922C>A	XP_011534286.1:p.Leu1308Met
XM_011535985.1:c.3742C>A	XP_011534287.1:p.Leu1248Met
XM_011535986.1:c.3502C>A	XP_011534288.1:p.Leu1168Met
XM_011535987.1:c.3121C>A	XP_011534289.1:p.Leu1041Met
XM_011535988.1:c.1984C>A	XP_011534290.1:p.Leu662Met
NM_001346813.1:c.4843C>A	NP_001333742.1:p.Leu1615Met
NM_001363725.1:c.2593C>A	NP_001350654.1:p.Leu865Met
XM_011535984.2:c.5053C>A	XP_011534286.2:p.Leu1685Met
XM_011535988.3:c.1984C>A	XP_011534290.1:p.Leu662Met
XM_017011103.2:c.4954C>A	XP_016866592.1:p.Leu1652Met
XM_017011104.1:c.4924C>A	XP_016866593.1:p.Leu1642Met
XM_017011105.2:c.4894C>A	XP_016866594.1:p.Leu1632Met
XM_017011106.2:c.4765C>A	XP_016866595.1:p.Leu1589Met
XM_017011107.2:c.4744C>A	XP_016866596.1:p.Leu1582Met
XR_002956289.1:n.5039C>A
NM_001363725.2:c.2593C>A	NP_001350654.1:p.Leu865Met
NM_001371656.1:c.4972C>A	NP_001358585.1:p.Leu1658Met
NM_001374820.1:c.4972C>A	NP_001361749.1:p.Leu1658Met
NM_001374828.1:c.5092C>A MANE Select	NP_001361757.1:p.Leu1698Met
NM_017519.3:c.4933C>A	NP_059989.3:p.Leu1645Met