Canonical Allele Identifier: CA366235070

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157190084-T-A
• MyVariant Identifiers: chr6:g.157511218T>A (hg19) ; chr6:g.157190084T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3946T>A	ENSP00000055163.8:p.Ser1316Thr
ENST00000414678.8:c.4015T>A	ENSP00000412835.3:p.Ser1339Thr
ENST00000637015.2:c.4234T>A	ENSP00000489729.2:p.Ser1412Thr
ENST00000346085.10:c.3985T>A	ENSP00000344546.5:p.Ser1329Thr
ENST00000350026.10:c.3697T>A	ENSP00000055163.7:p.Ser1233Thr
ENST00000414678.7:c.2263T>A	ENSP00000412835.2:p.Ser755Thr
ENST00000635849.1:c.1426T>A	ENSP00000490948.1:p.Ser476Thr
ENST00000635957.1:c.1057T>A	ENSP00000490385.1:p.Ser353Thr
ENST00000636930.2:c.4105T>A MANE Select	ENSP00000490491.2:p.Ser1369Thr
ENST00000636940.1:n.2102T>A
ENST00000637015.1:c.1473T>A
ENST00000637568.1:c.1387T>A
ENST00000637741.1:n.771T>A
ENST00000637810.1:c.1447T>A	ENSP00000489636.1:p.Ser483Thr
ENST00000637904.1:c.1606T>A	ENSP00000490550.1:p.Ser536Thr
ENST00000647938.1:c.3736T>A	ENSP00000498155.1:p.Ser1246Thr
ENST00000346085.9:c.3736T>A	ENSP00000344546.4:p.Ser1246Thr
ENST00000350026.9:c.3697T>A	ENSP00000055163.7:p.Ser1233Thr
ENST00000414678.6:c.2263T>A	ENSP00000412835.2:p.Ser755Thr
NM_017519.2:c.3697T>A	NP_059989.2:p.Ser1233Thr
NM_020732.3:c.3736T>A	NP_065783.3:p.Ser1246Thr
XM_005267069.3:c.3856T>A	XP_005267126.2:p.Ser1286Thr
XM_011535984.1:c.2935T>A	XP_011534286.1:p.Ser979Thr
XM_011535985.1:c.2755T>A	XP_011534287.1:p.Ser919Thr
XM_011535986.1:c.2515T>A	XP_011534288.1:p.Ser839Thr
XM_011535987.1:c.2134T>A	XP_011534289.1:p.Ser712Thr
XM_011535988.1:c.997T>A	XP_011534290.1:p.Ser333Thr
NM_001346813.1:c.3856T>A	NP_001333742.1:p.Ser1286Thr
NM_001363725.1:c.1606T>A	NP_001350654.1:p.Ser536Thr
XM_011535984.2:c.4066T>A	XP_011534286.2:p.Ser1356Thr
XM_011535988.3:c.997T>A	XP_011534290.1:p.Ser333Thr
XM_017011103.2:c.3967T>A	XP_016866592.1:p.Ser1323Thr
XM_017011104.1:c.3937T>A	XP_016866593.1:p.Ser1313Thr
XM_017011105.2:c.3907T>A	XP_016866594.1:p.Ser1303Thr
XM_017011106.2:c.3778T>A	XP_016866595.1:p.Ser1260Thr
XM_017011107.2:c.3757T>A	XP_016866596.1:p.Ser1253Thr
XR_002956289.1:n.4149T>A
NM_001363725.2:c.1606T>A	NP_001350654.1:p.Ser536Thr
NM_001371656.1:c.3985T>A	NP_001358585.1:p.Ser1329Thr
NM_001374820.1:c.3985T>A	NP_001361749.1:p.Ser1329Thr
NM_001374828.1:c.4105T>A MANE Select	NP_001361757.1:p.Ser1369Thr
NM_017519.3:c.3946T>A	NP_059989.3:p.Ser1316Thr