Canonical Allele Identifier: CA366234042

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510799C>T (hg19) ; chr6:g.157189665C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189665C>T , CM000668.2:g.157189665C>T	GRCh38
NC_000006.11:g.157510799C>T , CM000668.1:g.157510799C>T	GRCh37
NC_000006.10:g.157552491C>T	NCBI36
NG_032093.1:g.416736C>T
NG_032093.2:g.416736C>T
NG_066624.1:g.418640C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3784C>T	ENSP00000055163.8:p.Pro1262Ser
ENST00000414678.8:c.3853C>T	ENSP00000412835.3:p.Pro1285Ser
ENST00000637015.2:c.4072C>T	ENSP00000489729.2:p.Pro1358Ser
ENST00000346085.10:c.3823C>T	ENSP00000344546.5:p.Pro1275Ser
ENST00000350026.10:c.3535C>T	ENSP00000055163.7:p.Pro1179Ser
ENST00000414678.7:c.2101C>T	ENSP00000412835.2:p.Pro701Ser
ENST00000635849.1:c.1264C>T	ENSP00000490948.1:p.Pro422Ser
ENST00000635957.1:c.898C>T	ENSP00000490385.1:p.Pro300Ser
ENST00000636930.2:c.3943C>T MANE Select	ENSP00000490491.2:p.Pro1315Ser
ENST00000636940.1:n.1940C>T
ENST00000637015.1:c.1311C>T
ENST00000637568.1:c.1225C>T
ENST00000637741.1:n.609C>T
ENST00000637810.1:c.1285C>T	ENSP00000489636.1:p.Pro429Ser
ENST00000637904.1:c.1444C>T	ENSP00000490550.1:p.Pro482Ser
ENST00000647938.1:c.3574C>T	ENSP00000498155.1:p.Pro1192Ser
ENST00000346085.9:c.3574C>T	ENSP00000344546.4:p.Pro1192Ser
ENST00000350026.9:c.3535C>T	ENSP00000055163.7:p.Pro1179Ser
ENST00000414678.6:c.2101C>T	ENSP00000412835.2:p.Pro701Ser
NM_017519.2:c.3535C>T	NP_059989.2:p.Pro1179Ser
NM_020732.3:c.3574C>T	NP_065783.3:p.Pro1192Ser
XM_005267069.3:c.3694C>T	XP_005267126.2:p.Pro1232Ser
XM_011535984.1:c.2773C>T	XP_011534286.1:p.Pro925Ser
XM_011535985.1:c.2593C>T	XP_011534287.1:p.Pro865Ser
XM_011535986.1:c.2353C>T	XP_011534288.1:p.Pro785Ser
XM_011535987.1:c.1972C>T	XP_011534289.1:p.Pro658Ser
XM_011535988.1:c.835C>T	XP_011534290.1:p.Pro279Ser
NM_001346813.1:c.3694C>T	NP_001333742.1:p.Pro1232Ser
NM_001363725.1:c.1444C>T	NP_001350654.1:p.Pro482Ser
XM_011535984.2:c.3904C>T	XP_011534286.2:p.Pro1302Ser
XM_011535988.3:c.835C>T	XP_011534290.1:p.Pro279Ser
XM_017011103.2:c.3805C>T	XP_016866592.1:p.Pro1269Ser
XM_017011104.1:c.3775C>T	XP_016866593.1:p.Pro1259Ser
XM_017011105.2:c.3745C>T	XP_016866594.1:p.Pro1249Ser
XM_017011106.2:c.3616C>T	XP_016866595.1:p.Pro1206Ser
XM_017011107.2:c.3595C>T	XP_016866596.1:p.Pro1199Ser
XR_002956289.1:n.3987C>T
NM_001363725.2:c.1444C>T	NP_001350654.1:p.Pro482Ser
NM_001371656.1:c.3823C>T	NP_001358585.1:p.Pro1275Ser
NM_001374820.1:c.3823C>T	NP_001361749.1:p.Pro1275Ser
NM_001374828.1:c.3943C>T MANE Select	NP_001361757.1:p.Pro1315Ser
NM_017519.3:c.3784C>T	NP_059989.3:p.Pro1262Ser