Canonical Allele Identifier: CA366235303

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128339749
• MyVariant Identifiers: chr6:g.157511249C>T (hg19) ; chr6:g.157190115C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190115C>T , CM000668.2:g.157190115C>T	GRCh38
NC_000006.11:g.157511249C>T , CM000668.1:g.157511249C>T	GRCh37
NC_000006.10:g.157552941C>T	NCBI36
NG_032093.1:g.417186C>T
NG_032093.2:g.417186C>T
NG_066624.1:g.419090C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3977C>T	ENSP00000055163.8:p.Pro1326Leu
ENST00000414678.8:c.4046C>T	ENSP00000412835.3:p.Pro1349Leu
ENST00000637015.2:c.4265C>T	ENSP00000489729.2:p.Pro1422Leu
ENST00000346085.10:c.4016C>T	ENSP00000344546.5:p.Pro1339Leu
ENST00000350026.10:c.3728C>T	ENSP00000055163.7:p.Pro1243Leu
ENST00000414678.7:c.2294C>T	ENSP00000412835.2:p.Pro765Leu
ENST00000635849.1:c.1457C>T	ENSP00000490948.1:p.Pro486Leu
ENST00000635957.1:c.1088C>T	ENSP00000490385.1:p.Pro363Leu
ENST00000636930.2:c.4136C>T MANE Select	ENSP00000490491.2:p.Pro1379Leu
ENST00000636940.1:n.2133C>T
ENST00000637015.1:c.1504C>T
ENST00000637568.1:c.1418C>T
ENST00000637741.1:n.802C>T
ENST00000637810.1:c.1478C>T	ENSP00000489636.1:p.Pro493Leu
ENST00000637904.1:c.1637C>T	ENSP00000490550.1:p.Pro546Leu
ENST00000647938.1:c.3767C>T	ENSP00000498155.1:p.Pro1256Leu
ENST00000346085.9:c.3767C>T	ENSP00000344546.4:p.Pro1256Leu
ENST00000350026.9:c.3728C>T	ENSP00000055163.7:p.Pro1243Leu
ENST00000414678.6:c.2294C>T	ENSP00000412835.2:p.Pro765Leu
NM_017519.2:c.3728C>T	NP_059989.2:p.Pro1243Leu
NM_020732.3:c.3767C>T	NP_065783.3:p.Pro1256Leu
XM_005267069.3:c.3887C>T	XP_005267126.2:p.Pro1296Leu
XM_011535984.1:c.2966C>T	XP_011534286.1:p.Pro989Leu
XM_011535985.1:c.2786C>T	XP_011534287.1:p.Pro929Leu
XM_011535986.1:c.2546C>T	XP_011534288.1:p.Pro849Leu
XM_011535987.1:c.2165C>T	XP_011534289.1:p.Pro722Leu
XM_011535988.1:c.1028C>T	XP_011534290.1:p.Pro343Leu
NM_001346813.1:c.3887C>T	NP_001333742.1:p.Pro1296Leu
NM_001363725.1:c.1637C>T	NP_001350654.1:p.Pro546Leu
XM_011535984.2:c.4097C>T	XP_011534286.2:p.Pro1366Leu
XM_011535988.3:c.1028C>T	XP_011534290.1:p.Pro343Leu
XM_017011103.2:c.3998C>T	XP_016866592.1:p.Pro1333Leu
XM_017011104.1:c.3968C>T	XP_016866593.1:p.Pro1323Leu
XM_017011105.2:c.3938C>T	XP_016866594.1:p.Pro1313Leu
XM_017011106.2:c.3809C>T	XP_016866595.1:p.Pro1270Leu
XM_017011107.2:c.3788C>T	XP_016866596.1:p.Pro1263Leu
XR_002956289.1:n.4180C>T
NM_001363725.2:c.1637C>T	NP_001350654.1:p.Pro546Leu
NM_001371656.1:c.4016C>T	NP_001358585.1:p.Pro1339Leu
NM_001374820.1:c.4016C>T	NP_001361749.1:p.Pro1339Leu
NM_001374828.1:c.4136C>T MANE Select	NP_001361757.1:p.Pro1379Leu
NM_017519.3:c.3977C>T	NP_059989.3:p.Pro1326Leu