Canonical Allele Identifier: CA10602933

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 280708
• ClinVar RCV Id: RCV000276336 ; RCV001807205
• dbSNP Id: rs750447037
• MyVariant Identifiers: chr6:g.157527613C>T (hg19) ; chr6:g.157206479C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157206479C>T , CM000668.2:g.157206479C>T	GRCh38
NC_000006.11:g.157527613C>T , CM000668.1:g.157527613C>T	GRCh37
NC_000006.10:g.157569305C>T	NCBI36
NG_032093.1:g.433550C>T
NG_032093.2:g.433550C>T
NG_066624.1:g.435454C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.5548C>T	ENSP00000055163.8:p.Gln1850Ter
ENST00000414678.8:c.5617C>T	ENSP00000412835.3:p.Gln1873Ter
ENST00000637015.2:c.5836C>T	ENSP00000489729.2:p.Gln1946Ter
ENST00000346085.10:c.5587C>T	ENSP00000344546.5:p.Gln1863Ter
ENST00000350026.10:c.5299C>T	ENSP00000055163.7:p.Gln1767Ter
ENST00000414678.7:c.3865C>T	ENSP00000412835.2:p.Gln1289Ter
ENST00000635849.1:c.3028C>T	ENSP00000490948.1:p.Gln1010Ter
ENST00000635957.1:c.2659C>T	ENSP00000490385.1:p.Gln887Ter
ENST00000636227.1:n.4170C>T
ENST00000636254.1:n.1627C>T
ENST00000636930.2:c.5707C>T MANE Select	ENSP00000490491.2:p.Gln1903Ter
ENST00000636940.1:n.3704C>T
ENST00000637015.1:c.3075C>T
ENST00000637568.1:c.2989C>T
ENST00000637741.1:n.2373C>T
ENST00000637810.1:c.3049C>T	ENSP00000489636.1:p.Gln1017Ter
ENST00000637904.1:c.3208C>T	ENSP00000490550.1:p.Gln1070Ter
ENST00000637933.1:n.2822C>T
ENST00000647938.1:c.5338C>T	ENSP00000498155.1:p.Gln1780Ter
ENST00000346085.9:c.5338C>T	ENSP00000344546.4:p.Gln1780Ter
ENST00000350026.9:c.5299C>T	ENSP00000055163.7:p.Gln1767Ter
ENST00000414678.6:c.3865C>T	ENSP00000412835.2:p.Gln1289Ter
NM_017519.2:c.5299C>T	NP_059989.2:p.Gln1767Ter
NM_020732.3:c.5338C>T	NP_065783.3:p.Gln1780Ter
XM_005267069.3:c.5458C>T	XP_005267126.2:p.Gln1820Ter
XM_011535984.1:c.4537C>T	XP_011534286.1:p.Gln1513Ter
XM_011535985.1:c.4357C>T	XP_011534287.1:p.Gln1453Ter
XM_011535986.1:c.4117C>T	XP_011534288.1:p.Gln1373Ter
XM_011535987.1:c.3736C>T	XP_011534289.1:p.Gln1246Ter
XM_011535988.1:c.2599C>T	XP_011534290.1:p.Gln867Ter
NM_001346813.1:c.5458C>T	NP_001333742.1:p.Gln1820Ter
NM_001363725.1:c.3208C>T	NP_001350654.1:p.Gln1070Ter
XM_011535984.2:c.5668C>T	XP_011534286.2:p.Gln1890Ter
XM_011535988.3:c.2599C>T	XP_011534290.1:p.Gln867Ter
XM_017011103.2:c.5569C>T	XP_016866592.1:p.Gln1857Ter
XM_017011104.1:c.5539C>T	XP_016866593.1:p.Gln1847Ter
XM_017011105.2:c.5509C>T	XP_016866594.1:p.Gln1837Ter
XM_017011106.2:c.5380C>T	XP_016866595.1:p.Gln1794Ter
XM_017011107.2:c.5359C>T	XP_016866596.1:p.Gln1787Ter
XR_002956289.1:n.5654C>T
NM_001363725.2:c.3208C>T	NP_001350654.1:p.Gln1070Ter
NM_001371656.1:c.5587C>T	NP_001358585.1:p.Gln1863Ter
NM_001374820.1:c.5587C>T	NP_001361749.1:p.Gln1863Ter
NM_001374828.1:c.5707C>T MANE Select	NP_001361757.1:p.Gln1903Ter
NM_017519.3:c.5548C>T	NP_059989.3:p.Gln1850Ter