Canonical Allele Identifier: CA366235073

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511218T>G (hg19) ; chr6:g.157190084T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190084T>G , CM000668.2:g.157190084T>G	GRCh38
NC_000006.11:g.157511218T>G , CM000668.1:g.157511218T>G	GRCh37
NC_000006.10:g.157552910T>G	NCBI36
NG_032093.1:g.417155T>G
NG_032093.2:g.417155T>G
NG_066624.1:g.419059T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3946T>G	ENSP00000055163.8:p.Ser1316Ala
ENST00000414678.8:c.4015T>G	ENSP00000412835.3:p.Ser1339Ala
ENST00000637015.2:c.4234T>G	ENSP00000489729.2:p.Ser1412Ala
ENST00000346085.10:c.3985T>G	ENSP00000344546.5:p.Ser1329Ala
ENST00000350026.10:c.3697T>G	ENSP00000055163.7:p.Ser1233Ala
ENST00000414678.7:c.2263T>G	ENSP00000412835.2:p.Ser755Ala
ENST00000635849.1:c.1426T>G	ENSP00000490948.1:p.Ser476Ala
ENST00000635957.1:c.1057T>G	ENSP00000490385.1:p.Ser353Ala
ENST00000636930.2:c.4105T>G MANE Select	ENSP00000490491.2:p.Ser1369Ala
ENST00000636940.1:n.2102T>G
ENST00000637015.1:c.1473T>G
ENST00000637568.1:c.1387T>G
ENST00000637741.1:n.771T>G
ENST00000637810.1:c.1447T>G	ENSP00000489636.1:p.Ser483Ala
ENST00000637904.1:c.1606T>G	ENSP00000490550.1:p.Ser536Ala
ENST00000647938.1:c.3736T>G	ENSP00000498155.1:p.Ser1246Ala
ENST00000346085.9:c.3736T>G	ENSP00000344546.4:p.Ser1246Ala
ENST00000350026.9:c.3697T>G	ENSP00000055163.7:p.Ser1233Ala
ENST00000414678.6:c.2263T>G	ENSP00000412835.2:p.Ser755Ala
NM_017519.2:c.3697T>G	NP_059989.2:p.Ser1233Ala
NM_020732.3:c.3736T>G	NP_065783.3:p.Ser1246Ala
XM_005267069.3:c.3856T>G	XP_005267126.2:p.Ser1286Ala
XM_011535984.1:c.2935T>G	XP_011534286.1:p.Ser979Ala
XM_011535985.1:c.2755T>G	XP_011534287.1:p.Ser919Ala
XM_011535986.1:c.2515T>G	XP_011534288.1:p.Ser839Ala
XM_011535987.1:c.2134T>G	XP_011534289.1:p.Ser712Ala
XM_011535988.1:c.997T>G	XP_011534290.1:p.Ser333Ala
NM_001346813.1:c.3856T>G	NP_001333742.1:p.Ser1286Ala
NM_001363725.1:c.1606T>G	NP_001350654.1:p.Ser536Ala
XM_011535984.2:c.4066T>G	XP_011534286.2:p.Ser1356Ala
XM_011535988.3:c.997T>G	XP_011534290.1:p.Ser333Ala
XM_017011103.2:c.3967T>G	XP_016866592.1:p.Ser1323Ala
XM_017011104.1:c.3937T>G	XP_016866593.1:p.Ser1313Ala
XM_017011105.2:c.3907T>G	XP_016866594.1:p.Ser1303Ala
XM_017011106.2:c.3778T>G	XP_016866595.1:p.Ser1260Ala
XM_017011107.2:c.3757T>G	XP_016866596.1:p.Ser1253Ala
XR_002956289.1:n.4149T>G
NM_001363725.2:c.1606T>G	NP_001350654.1:p.Ser536Ala
NM_001371656.1:c.3985T>G	NP_001358585.1:p.Ser1329Ala
NM_001374820.1:c.3985T>G	NP_001361749.1:p.Ser1329Ala
NM_001374828.1:c.4105T>G MANE Select	NP_001361757.1:p.Ser1369Ala
NM_017519.3:c.3946T>G	NP_059989.3:p.Ser1316Ala