Canonical Allele Identifier: CA366234020

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510790T>A (hg19) ; chr6:g.157189656T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189656T>A , CM000668.2:g.157189656T>A	GRCh38
NC_000006.11:g.157510790T>A , CM000668.1:g.157510790T>A	GRCh37
NC_000006.10:g.157552482T>A	NCBI36
NG_032093.1:g.416727T>A
NG_032093.2:g.416727T>A
NG_066624.1:g.418631T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3775T>A	ENSP00000055163.8:p.Leu1259Met
ENST00000414678.8:c.3844T>A	ENSP00000412835.3:p.Leu1282Met
ENST00000637015.2:c.4063T>A	ENSP00000489729.2:p.Leu1355Met
ENST00000346085.10:c.3814T>A	ENSP00000344546.5:p.Leu1272Met
ENST00000350026.10:c.3526T>A	ENSP00000055163.7:p.Leu1176Met
ENST00000414678.7:c.2092T>A	ENSP00000412835.2:p.Leu698Met
ENST00000635849.1:c.1255T>A	ENSP00000490948.1:p.Leu419Met
ENST00000635957.1:c.889T>A	ENSP00000490385.1:p.Leu297Met
ENST00000636930.2:c.3934T>A MANE Select	ENSP00000490491.2:p.Leu1312Met
ENST00000636940.1:n.1931T>A
ENST00000637015.1:c.1302T>A
ENST00000637568.1:c.1216T>A
ENST00000637741.1:n.600T>A
ENST00000637810.1:c.1276T>A	ENSP00000489636.1:p.Leu426Met
ENST00000637904.1:c.1435T>A	ENSP00000490550.1:p.Leu479Met
ENST00000647938.1:c.3565T>A	ENSP00000498155.1:p.Leu1189Met
ENST00000346085.9:c.3565T>A	ENSP00000344546.4:p.Leu1189Met
ENST00000350026.9:c.3526T>A	ENSP00000055163.7:p.Leu1176Met
ENST00000414678.6:c.2092T>A	ENSP00000412835.2:p.Leu698Met
NM_017519.2:c.3526T>A	NP_059989.2:p.Leu1176Met
NM_020732.3:c.3565T>A	NP_065783.3:p.Leu1189Met
XM_005267069.3:c.3685T>A	XP_005267126.2:p.Leu1229Met
XM_011535984.1:c.2764T>A	XP_011534286.1:p.Leu922Met
XM_011535985.1:c.2584T>A	XP_011534287.1:p.Leu862Met
XM_011535986.1:c.2344T>A	XP_011534288.1:p.Leu782Met
XM_011535987.1:c.1963T>A	XP_011534289.1:p.Leu655Met
XM_011535988.1:c.826T>A	XP_011534290.1:p.Leu276Met
NM_001346813.1:c.3685T>A	NP_001333742.1:p.Leu1229Met
NM_001363725.1:c.1435T>A	NP_001350654.1:p.Leu479Met
XM_011535984.2:c.3895T>A	XP_011534286.2:p.Leu1299Met
XM_011535988.3:c.826T>A	XP_011534290.1:p.Leu276Met
XM_017011103.2:c.3796T>A	XP_016866592.1:p.Leu1266Met
XM_017011104.1:c.3766T>A	XP_016866593.1:p.Leu1256Met
XM_017011105.2:c.3736T>A	XP_016866594.1:p.Leu1246Met
XM_017011106.2:c.3607T>A	XP_016866595.1:p.Leu1203Met
XM_017011107.2:c.3586T>A	XP_016866596.1:p.Leu1196Met
XR_002956289.1:n.3978T>A
NM_001363725.2:c.1435T>A	NP_001350654.1:p.Leu479Met
NM_001371656.1:c.3814T>A	NP_001358585.1:p.Leu1272Met
NM_001374820.1:c.3814T>A	NP_001361749.1:p.Leu1272Met
NM_001374828.1:c.3934T>A MANE Select	NP_001361757.1:p.Leu1312Met
NM_017519.3:c.3775T>A	NP_059989.3:p.Leu1259Met