Canonical Allele Identifier: CA209106

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 210306
• ClinVar RCV Id: RCV000194737 ; RCV000523275 ; RCV000735324 ; RCV003156084
• dbSNP Id: rs797045283
• COSMIC: COSM216002
• MyVariant Identifiers: chr6:g.157528243C>T (hg19) ; chr6:g.157207109C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207109C>T , CM000668.2:g.157207109C>T	GRCh38
NC_000006.11:g.157528243C>T , CM000668.1:g.157528243C>T	GRCh37
NC_000006.10:g.157569935C>T	NCBI36
NG_032093.1:g.434180C>T
NG_032093.2:g.434180C>T
NG_066624.1:g.436084C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.6178C>T	ENSP00000055163.8:p.Arg2060Ter
ENST00000414678.8:c.6247C>T	ENSP00000412835.3:p.Arg2083Ter
ENST00000637015.2:c.6466C>T	ENSP00000489729.2:p.Arg2156Ter
ENST00000346085.10:c.6217C>T	ENSP00000344546.5:p.Arg2073Ter
ENST00000350026.10:c.5929C>T	ENSP00000055163.7:p.Arg1977Ter
ENST00000414678.7:c.4495C>T	ENSP00000412835.2:p.Arg1499Ter
ENST00000635849.1:c.3658C>T	ENSP00000490948.1:p.Arg1220Ter
ENST00000635928.1:c.493C>T	ENSP00000489717.1:p.Arg165Ter
ENST00000635957.1:c.3289C>T	ENSP00000490385.1:p.Arg1097Ter
ENST00000636227.1:n.4800C>T
ENST00000636254.1:n.2257C>T
ENST00000636930.2:c.6337C>T MANE Select	ENSP00000490491.2:p.Arg2113Ter
ENST00000636940.1:n.4334C>T
ENST00000637015.1:c.3705C>T
ENST00000637568.1:c.3619C>T
ENST00000637741.1:n.3003C>T
ENST00000637810.1:c.3679C>T	ENSP00000489636.1:p.Arg1227Ter
ENST00000637904.1:c.3838C>T	ENSP00000490550.1:p.Arg1280Ter
ENST00000637933.1:n.3452C>T
ENST00000647938.1:c.5968C>T	ENSP00000498155.1:p.Arg1990Ter
ENST00000346085.9:c.5968C>T	ENSP00000344546.4:p.Arg1990Ter
ENST00000350026.9:c.5929C>T	ENSP00000055163.7:p.Arg1977Ter
ENST00000414678.6:c.4495C>T	ENSP00000412835.2:p.Arg1499Ter
NM_017519.2:c.5929C>T	NP_059989.2:p.Arg1977Ter
NM_020732.3:c.5968C>T	NP_065783.3:p.Arg1990Ter
XM_005267069.3:c.6088C>T	XP_005267126.2:p.Arg2030Ter
XM_011535984.1:c.5167C>T	XP_011534286.1:p.Arg1723Ter
XM_011535985.1:c.4987C>T	XP_011534287.1:p.Arg1663Ter
XM_011535986.1:c.4747C>T	XP_011534288.1:p.Arg1583Ter
XM_011535987.1:c.4366C>T	XP_011534289.1:p.Arg1456Ter
XM_011535988.1:c.3229C>T	XP_011534290.1:p.Arg1077Ter
NM_001346813.1:c.6088C>T	NP_001333742.1:p.Arg2030Ter
NM_001363725.1:c.3838C>T	NP_001350654.1:p.Arg1280Ter
XM_011535984.2:c.6298C>T	XP_011534286.2:p.Arg2100Ter
XM_011535988.3:c.3229C>T	XP_011534290.1:p.Arg1077Ter
XM_017011103.2:c.6199C>T	XP_016866592.1:p.Arg2067Ter
XM_017011104.1:c.6169C>T	XP_016866593.1:p.Arg2057Ter
XM_017011105.2:c.6139C>T	XP_016866594.1:p.Arg2047Ter
XM_017011106.2:c.6010C>T	XP_016866595.1:p.Arg2004Ter
XM_017011107.2:c.5989C>T	XP_016866596.1:p.Arg1997Ter
XR_002956289.1:n.6284C>T
NM_001363725.2:c.3838C>T	NP_001350654.1:p.Arg1280Ter
NM_001371656.1:c.6217C>T	NP_001358585.1:p.Arg2073Ter
NM_001374820.1:c.6217C>T	NP_001361749.1:p.Arg2073Ter
NM_001374828.1:c.6337C>T MANE Select	NP_001361757.1:p.Arg2113Ter
NM_017519.3:c.6178C>T	NP_059989.3:p.Arg2060Ter