Canonical Allele Identifier: CA366234104

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510829T>A (hg19) ; chr6:g.157189695T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189695T>A , CM000668.2:g.157189695T>A	GRCh38
NC_000006.11:g.157510829T>A , CM000668.1:g.157510829T>A	GRCh37
NC_000006.10:g.157552521T>A	NCBI36
NG_032093.1:g.416766T>A
NG_032093.2:g.416766T>A
NG_066624.1:g.418670T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3814T>A	ENSP00000055163.8:p.Ser1272Thr
ENST00000414678.8:c.3883T>A	ENSP00000412835.3:p.Ser1295Thr
ENST00000637015.2:c.4102T>A	ENSP00000489729.2:p.Ser1368Thr
ENST00000346085.10:c.3853T>A	ENSP00000344546.5:p.Ser1285Thr
ENST00000350026.10:c.3565T>A	ENSP00000055163.7:p.Ser1189Thr
ENST00000414678.7:c.2131T>A	ENSP00000412835.2:p.Ser711Thr
ENST00000635849.1:c.1294T>A	ENSP00000490948.1:p.Ser432Thr
ENST00000635957.1:c.928T>A	ENSP00000490385.1:p.Ser310Thr
ENST00000636930.2:c.3973T>A MANE Select	ENSP00000490491.2:p.Ser1325Thr
ENST00000636940.1:n.1970T>A
ENST00000637015.1:c.1341T>A
ENST00000637568.1:c.1255T>A
ENST00000637741.1:n.639T>A
ENST00000637810.1:c.1315T>A	ENSP00000489636.1:p.Ser439Thr
ENST00000637904.1:c.1474T>A	ENSP00000490550.1:p.Ser492Thr
ENST00000647938.1:c.3604T>A	ENSP00000498155.1:p.Ser1202Thr
ENST00000346085.9:c.3604T>A	ENSP00000344546.4:p.Ser1202Thr
ENST00000350026.9:c.3565T>A	ENSP00000055163.7:p.Ser1189Thr
ENST00000414678.6:c.2131T>A	ENSP00000412835.2:p.Ser711Thr
NM_017519.2:c.3565T>A	NP_059989.2:p.Ser1189Thr
NM_020732.3:c.3604T>A	NP_065783.3:p.Ser1202Thr
XM_005267069.3:c.3724T>A	XP_005267126.2:p.Ser1242Thr
XM_011535984.1:c.2803T>A	XP_011534286.1:p.Ser935Thr
XM_011535985.1:c.2623T>A	XP_011534287.1:p.Ser875Thr
XM_011535986.1:c.2383T>A	XP_011534288.1:p.Ser795Thr
XM_011535987.1:c.2002T>A	XP_011534289.1:p.Ser668Thr
XM_011535988.1:c.865T>A	XP_011534290.1:p.Ser289Thr
NM_001346813.1:c.3724T>A	NP_001333742.1:p.Ser1242Thr
NM_001363725.1:c.1474T>A	NP_001350654.1:p.Ser492Thr
XM_011535984.2:c.3934T>A	XP_011534286.2:p.Ser1312Thr
XM_011535988.3:c.865T>A	XP_011534290.1:p.Ser289Thr
XM_017011103.2:c.3835T>A	XP_016866592.1:p.Ser1279Thr
XM_017011104.1:c.3805T>A	XP_016866593.1:p.Ser1269Thr
XM_017011105.2:c.3775T>A	XP_016866594.1:p.Ser1259Thr
XM_017011106.2:c.3646T>A	XP_016866595.1:p.Ser1216Thr
XM_017011107.2:c.3625T>A	XP_016866596.1:p.Ser1209Thr
XR_002956289.1:n.4017T>A
NM_001363725.2:c.1474T>A	NP_001350654.1:p.Ser492Thr
NM_001371656.1:c.3853T>A	NP_001358585.1:p.Ser1285Thr
NM_001374820.1:c.3853T>A	NP_001361749.1:p.Ser1285Thr
NM_001374828.1:c.3973T>A MANE Select	NP_001361757.1:p.Ser1325Thr
NM_017519.3:c.3814T>A	NP_059989.3:p.Ser1272Thr