Canonical Allele Identifier: CA366234157

Gene: ARID1B

Linked Data

• dbSNP Id: rs138482029
• MyVariant Identifiers: chr6:g.157510853C>A (hg19) ; chr6:g.157189719C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189719C>A , CM000668.2:g.157189719C>A	GRCh38
NC_000006.11:g.157510853C>A , CM000668.1:g.157510853C>A	GRCh37
NC_000006.10:g.157552545C>A	NCBI36
NG_032093.1:g.416790C>A
NG_032093.2:g.416790C>A
NG_066624.1:g.418694C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3838C>A	ENSP00000055163.8:p.Leu1280Met
ENST00000414678.8:c.3907C>A	ENSP00000412835.3:p.Leu1303Met
ENST00000637015.2:c.4126C>A	ENSP00000489729.2:p.Leu1376Met
ENST00000346085.10:c.3877C>A	ENSP00000344546.5:p.Leu1293Met
ENST00000350026.10:c.3589C>A	ENSP00000055163.7:p.Leu1197Met
ENST00000414678.7:c.2155C>A	ENSP00000412835.2:p.Leu719Met
ENST00000635849.1:c.1318C>A	ENSP00000490948.1:p.Leu440Met
ENST00000635957.1:c.952C>A	ENSP00000490385.1:p.Leu318Met
ENST00000636930.2:c.3997C>A MANE Select	ENSP00000490491.2:p.Leu1333Met
ENST00000636940.1:n.1994C>A
ENST00000637015.1:c.1365C>A
ENST00000637568.1:c.1279C>A
ENST00000637741.1:n.663C>A
ENST00000637810.1:c.1339C>A	ENSP00000489636.1:p.Leu447Met
ENST00000637904.1:c.1498C>A	ENSP00000490550.1:p.Leu500Met
ENST00000647938.1:c.3628C>A	ENSP00000498155.1:p.Leu1210Met
ENST00000346085.9:c.3628C>A	ENSP00000344546.4:p.Leu1210Met
ENST00000350026.9:c.3589C>A	ENSP00000055163.7:p.Leu1197Met
ENST00000414678.6:c.2155C>A	ENSP00000412835.2:p.Leu719Met
NM_017519.2:c.3589C>A	NP_059989.2:p.Leu1197Met
NM_020732.3:c.3628C>A	NP_065783.3:p.Leu1210Met
XM_005267069.3:c.3748C>A	XP_005267126.2:p.Leu1250Met
XM_011535984.1:c.2827C>A	XP_011534286.1:p.Leu943Met
XM_011535985.1:c.2647C>A	XP_011534287.1:p.Leu883Met
XM_011535986.1:c.2407C>A	XP_011534288.1:p.Leu803Met
XM_011535987.1:c.2026C>A	XP_011534289.1:p.Leu676Met
XM_011535988.1:c.889C>A	XP_011534290.1:p.Leu297Met
NM_001346813.1:c.3748C>A	NP_001333742.1:p.Leu1250Met
NM_001363725.1:c.1498C>A	NP_001350654.1:p.Leu500Met
XM_011535984.2:c.3958C>A	XP_011534286.2:p.Leu1320Met
XM_011535988.3:c.889C>A	XP_011534290.1:p.Leu297Met
XM_017011103.2:c.3859C>A	XP_016866592.1:p.Leu1287Met
XM_017011104.1:c.3829C>A	XP_016866593.1:p.Leu1277Met
XM_017011105.2:c.3799C>A	XP_016866594.1:p.Leu1267Met
XM_017011106.2:c.3670C>A	XP_016866595.1:p.Leu1224Met
XM_017011107.2:c.3649C>A	XP_016866596.1:p.Leu1217Met
XR_002956289.1:n.4041C>A
NM_001363725.2:c.1498C>A	NP_001350654.1:p.Leu500Met
NM_001371656.1:c.3877C>A	NP_001358585.1:p.Leu1293Met
NM_001374820.1:c.3877C>A	NP_001361749.1:p.Leu1293Met
NM_001374828.1:c.3997C>A MANE Select	NP_001361757.1:p.Leu1333Met
NM_017519.3:c.3838C>A	NP_059989.3:p.Leu1280Met