Canonical Allele Identifier: CA366234185

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510868C>T (hg19) ; chr6:g.157189734C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189734C>T , CM000668.2:g.157189734C>T	GRCh38
NC_000006.11:g.157510868C>T , CM000668.1:g.157510868C>T	GRCh37
NC_000006.10:g.157552560C>T	NCBI36
NG_032093.1:g.416805C>T
NG_032093.2:g.416805C>T
NG_066624.1:g.418709C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3853C>T	ENSP00000055163.8:p.Pro1285Ser
ENST00000414678.8:c.3922C>T	ENSP00000412835.3:p.Pro1308Ser
ENST00000637015.2:c.4141C>T	ENSP00000489729.2:p.Pro1381Ser
ENST00000346085.10:c.3892C>T	ENSP00000344546.5:p.Pro1298Ser
ENST00000350026.10:c.3604C>T	ENSP00000055163.7:p.Pro1202Ser
ENST00000414678.7:c.2170C>T	ENSP00000412835.2:p.Pro724Ser
ENST00000635849.1:c.1333C>T	ENSP00000490948.1:p.Pro445Ser
ENST00000635957.1:c.967C>T	ENSP00000490385.1:p.Pro323Ser
ENST00000636930.2:c.4012C>T MANE Select	ENSP00000490491.2:p.Pro1338Ser
ENST00000636940.1:n.2009C>T
ENST00000637015.1:c.1380C>T
ENST00000637568.1:c.1294C>T
ENST00000637741.1:n.678C>T
ENST00000637810.1:c.1354C>T	ENSP00000489636.1:p.Pro452Ser
ENST00000637904.1:c.1513C>T	ENSP00000490550.1:p.Pro505Ser
ENST00000647938.1:c.3643C>T	ENSP00000498155.1:p.Pro1215Ser
ENST00000346085.9:c.3643C>T	ENSP00000344546.4:p.Pro1215Ser
ENST00000350026.9:c.3604C>T	ENSP00000055163.7:p.Pro1202Ser
ENST00000414678.6:c.2170C>T	ENSP00000412835.2:p.Pro724Ser
NM_017519.2:c.3604C>T	NP_059989.2:p.Pro1202Ser
NM_020732.3:c.3643C>T	NP_065783.3:p.Pro1215Ser
XM_005267069.3:c.3763C>T	XP_005267126.2:p.Pro1255Ser
XM_011535984.1:c.2842C>T	XP_011534286.1:p.Pro948Ser
XM_011535985.1:c.2662C>T	XP_011534287.1:p.Pro888Ser
XM_011535986.1:c.2422C>T	XP_011534288.1:p.Pro808Ser
XM_011535987.1:c.2041C>T	XP_011534289.1:p.Pro681Ser
XM_011535988.1:c.904C>T	XP_011534290.1:p.Pro302Ser
NM_001346813.1:c.3763C>T	NP_001333742.1:p.Pro1255Ser
NM_001363725.1:c.1513C>T	NP_001350654.1:p.Pro505Ser
XM_011535984.2:c.3973C>T	XP_011534286.2:p.Pro1325Ser
XM_011535988.3:c.904C>T	XP_011534290.1:p.Pro302Ser
XM_017011103.2:c.3874C>T	XP_016866592.1:p.Pro1292Ser
XM_017011104.1:c.3844C>T	XP_016866593.1:p.Pro1282Ser
XM_017011105.2:c.3814C>T	XP_016866594.1:p.Pro1272Ser
XM_017011106.2:c.3685C>T	XP_016866595.1:p.Pro1229Ser
XM_017011107.2:c.3664C>T	XP_016866596.1:p.Pro1222Ser
XR_002956289.1:n.4056C>T
NM_001363725.2:c.1513C>T	NP_001350654.1:p.Pro505Ser
NM_001371656.1:c.3892C>T	NP_001358585.1:p.Pro1298Ser
NM_001374820.1:c.3892C>T	NP_001361749.1:p.Pro1298Ser
NM_001374828.1:c.4012C>T MANE Select	NP_001361757.1:p.Pro1338Ser
NM_017519.3:c.3853C>T	NP_059989.3:p.Pro1285Ser