Canonical Allele Identifier: CA366234105

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3814T>C	ENSP00000055163.8:p.Ser1272Pro
ENST00000414678.8:c.3883T>C	ENSP00000412835.3:p.Ser1295Pro
ENST00000637015.2:c.4102T>C	ENSP00000489729.2:p.Ser1368Pro
ENST00000346085.10:c.3853T>C	ENSP00000344546.5:p.Ser1285Pro
ENST00000350026.10:c.3565T>C	ENSP00000055163.7:p.Ser1189Pro
ENST00000414678.7:c.2131T>C	ENSP00000412835.2:p.Ser711Pro
ENST00000635849.1:c.1294T>C	ENSP00000490948.1:p.Ser432Pro
ENST00000635957.1:c.928T>C	ENSP00000490385.1:p.Ser310Pro
ENST00000636930.2:c.3973T>C MANE Select	ENSP00000490491.2:p.Ser1325Pro
ENST00000636940.1:n.1970T>C
ENST00000637015.1:c.1341T>C
ENST00000637568.1:c.1255T>C
ENST00000637741.1:n.639T>C
ENST00000637810.1:c.1315T>C	ENSP00000489636.1:p.Ser439Pro
ENST00000637904.1:c.1474T>C	ENSP00000490550.1:p.Ser492Pro
ENST00000647938.1:c.3604T>C	ENSP00000498155.1:p.Ser1202Pro
ENST00000346085.9:c.3604T>C	ENSP00000344546.4:p.Ser1202Pro
ENST00000350026.9:c.3565T>C	ENSP00000055163.7:p.Ser1189Pro
ENST00000414678.6:c.2131T>C	ENSP00000412835.2:p.Ser711Pro
NM_017519.2:c.3565T>C	NP_059989.2:p.Ser1189Pro
NM_020732.3:c.3604T>C	NP_065783.3:p.Ser1202Pro
XM_005267069.3:c.3724T>C	XP_005267126.2:p.Ser1242Pro
XM_011535984.1:c.2803T>C	XP_011534286.1:p.Ser935Pro
XM_011535985.1:c.2623T>C	XP_011534287.1:p.Ser875Pro
XM_011535986.1:c.2383T>C	XP_011534288.1:p.Ser795Pro
XM_011535987.1:c.2002T>C	XP_011534289.1:p.Ser668Pro
XM_011535988.1:c.865T>C	XP_011534290.1:p.Ser289Pro
NM_001346813.1:c.3724T>C	NP_001333742.1:p.Ser1242Pro
NM_001363725.1:c.1474T>C	NP_001350654.1:p.Ser492Pro
XM_011535984.2:c.3934T>C	XP_011534286.2:p.Ser1312Pro
XM_011535988.3:c.865T>C	XP_011534290.1:p.Ser289Pro
XM_017011103.2:c.3835T>C	XP_016866592.1:p.Ser1279Pro
XM_017011104.1:c.3805T>C	XP_016866593.1:p.Ser1269Pro
XM_017011105.2:c.3775T>C	XP_016866594.1:p.Ser1259Pro
XM_017011106.2:c.3646T>C	XP_016866595.1:p.Ser1216Pro
XM_017011107.2:c.3625T>C	XP_016866596.1:p.Ser1209Pro
XR_002956289.1:n.4017T>C
NM_001363725.2:c.1474T>C	NP_001350654.1:p.Ser492Pro
NM_001371656.1:c.3853T>C	NP_001358585.1:p.Ser1285Pro
NM_001374820.1:c.3853T>C	NP_001361749.1:p.Ser1285Pro
NM_001374828.1:c.3973T>C MANE Select	NP_001361757.1:p.Ser1325Pro
NM_017519.3:c.3814T>C	NP_059989.3:p.Ser1272Pro