Canonical Allele Identifier: CA366242833

Gene: ARID1B

Linked Data

• dbSNP Id: rs1794109482
• MyVariant Identifiers: chr6:g.157522514C>T (hg19) ; chr6:g.157201380C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201380C>T , CM000668.2:g.157201380C>T	GRCh38
NC_000006.11:g.157522514C>T , CM000668.1:g.157522514C>T	GRCh37
NC_000006.10:g.157564206C>T	NCBI36
NG_032093.1:g.428451C>T
NG_032093.2:g.428451C>T
NG_066624.1:g.430355C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4996C>T	ENSP00000055163.8:p.Pro1666Ser
ENST00000414678.8:c.5065C>T	ENSP00000412835.3:p.Pro1689Ser
ENST00000637015.2:c.5284C>T	ENSP00000489729.2:p.Pro1762Ser
ENST00000346085.10:c.5035C>T	ENSP00000344546.5:p.Pro1679Ser
ENST00000350026.10:c.4747C>T	ENSP00000055163.7:p.Pro1583Ser
ENST00000414678.7:c.3313C>T	ENSP00000412835.2:p.Pro1105Ser
ENST00000635849.1:c.2476C>T	ENSP00000490948.1:p.Pro826Ser
ENST00000635957.1:c.2107C>T	ENSP00000490385.1:p.Pro703Ser
ENST00000636227.1:n.3618C>T
ENST00000636254.1:n.1075C>T
ENST00000636930.2:c.5155C>T MANE Select	ENSP00000490491.2:p.Pro1719Ser
ENST00000636940.1:n.3152C>T
ENST00000637015.1:c.2523C>T
ENST00000637568.1:c.2437C>T
ENST00000637741.1:n.1821C>T
ENST00000637810.1:c.2497C>T	ENSP00000489636.1:p.Pro833Ser
ENST00000637904.1:c.2656C>T	ENSP00000490550.1:p.Pro886Ser
ENST00000647938.1:c.4786C>T	ENSP00000498155.1:p.Pro1596Ser
ENST00000346085.9:c.4786C>T	ENSP00000344546.4:p.Pro1596Ser
ENST00000350026.9:c.4747C>T	ENSP00000055163.7:p.Pro1583Ser
ENST00000414678.6:c.3313C>T	ENSP00000412835.2:p.Pro1105Ser
NM_017519.2:c.4747C>T	NP_059989.2:p.Pro1583Ser
NM_020732.3:c.4786C>T	NP_065783.3:p.Pro1596Ser
XM_005267069.3:c.4906C>T	XP_005267126.2:p.Pro1636Ser
XM_011535984.1:c.3985C>T	XP_011534286.1:p.Pro1329Ser
XM_011535985.1:c.3805C>T	XP_011534287.1:p.Pro1269Ser
XM_011535986.1:c.3565C>T	XP_011534288.1:p.Pro1189Ser
XM_011535987.1:c.3184C>T	XP_011534289.1:p.Pro1062Ser
XM_011535988.1:c.2047C>T	XP_011534290.1:p.Pro683Ser
NM_001346813.1:c.4906C>T	NP_001333742.1:p.Pro1636Ser
NM_001363725.1:c.2656C>T	NP_001350654.1:p.Pro886Ser
XM_011535984.2:c.5116C>T	XP_011534286.2:p.Pro1706Ser
XM_011535988.3:c.2047C>T	XP_011534290.1:p.Pro683Ser
XM_017011103.2:c.5017C>T	XP_016866592.1:p.Pro1673Ser
XM_017011104.1:c.4987C>T	XP_016866593.1:p.Pro1663Ser
XM_017011105.2:c.4957C>T	XP_016866594.1:p.Pro1653Ser
XM_017011106.2:c.4828C>T	XP_016866595.1:p.Pro1610Ser
XM_017011107.2:c.4807C>T	XP_016866596.1:p.Pro1603Ser
XR_002956289.1:n.5102C>T
NM_001363725.2:c.2656C>T	NP_001350654.1:p.Pro886Ser
NM_001371656.1:c.5035C>T	NP_001358585.1:p.Pro1679Ser
NM_001374820.1:c.5035C>T	NP_001361749.1:p.Pro1679Ser
NM_001374828.1:c.5155C>T MANE Select	NP_001361757.1:p.Pro1719Ser
NM_017519.3:c.4996C>T	NP_059989.3:p.Pro1666Ser