Canonical Allele Identifier: CA366242378

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1709913
• ClinVar RCV Id: RCV002290255 ; RCV003120883
• dbSNP Id: rs1554235916
• MyVariant Identifiers: chr6:g.157522406C>T (hg19) ; chr6:g.157201272C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201272C>T , CM000668.2:g.157201272C>T	GRCh38
NC_000006.11:g.157522406C>T , CM000668.1:g.157522406C>T	GRCh37
NC_000006.10:g.157564098C>T	NCBI36
NG_032093.1:g.428343C>T
NG_032093.2:g.428343C>T
NG_066624.1:g.430247C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4888C>T	ENSP00000055163.8:p.Gln1630Ter
ENST00000414678.8:c.4957C>T	ENSP00000412835.3:p.Gln1653Ter
ENST00000637015.2:c.5176C>T	ENSP00000489729.2:p.Gln1726Ter
ENST00000346085.10:c.4927C>T	ENSP00000344546.5:p.Gln1643Ter
ENST00000350026.10:c.4639C>T	ENSP00000055163.7:p.Gln1547Ter
ENST00000414678.7:c.3205C>T	ENSP00000412835.2:p.Gln1069Ter
ENST00000635849.1:c.2368C>T	ENSP00000490948.1:p.Gln790Ter
ENST00000635957.1:c.1999C>T	ENSP00000490385.1:p.Gln667Ter
ENST00000636227.1:n.3510C>T
ENST00000636254.1:n.967C>T
ENST00000636930.2:c.5047C>T MANE Select	ENSP00000490491.2:p.Gln1683Ter
ENST00000636940.1:n.3044C>T
ENST00000637015.1:c.2415C>T
ENST00000637568.1:c.2329C>T
ENST00000637741.1:n.1713C>T
ENST00000637810.1:c.2389C>T	ENSP00000489636.1:p.Gln797Ter
ENST00000637904.1:c.2548C>T	ENSP00000490550.1:p.Gln850Ter
ENST00000647938.1:c.4678C>T	ENSP00000498155.1:p.Gln1560Ter
ENST00000346085.9:c.4678C>T	ENSP00000344546.4:p.Gln1560Ter
ENST00000350026.9:c.4639C>T	ENSP00000055163.7:p.Gln1547Ter
ENST00000414678.6:c.3205C>T	ENSP00000412835.2:p.Gln1069Ter
NM_017519.2:c.4639C>T	NP_059989.2:p.Gln1547Ter
NM_020732.3:c.4678C>T	NP_065783.3:p.Gln1560Ter
XM_005267069.3:c.4798C>T	XP_005267126.2:p.Gln1600Ter
XM_011535984.1:c.3877C>T	XP_011534286.1:p.Gln1293Ter
XM_011535985.1:c.3697C>T	XP_011534287.1:p.Gln1233Ter
XM_011535986.1:c.3457C>T	XP_011534288.1:p.Gln1153Ter
XM_011535987.1:c.3076C>T	XP_011534289.1:p.Gln1026Ter
XM_011535988.1:c.1939C>T	XP_011534290.1:p.Gln647Ter
NM_001346813.1:c.4798C>T	NP_001333742.1:p.Gln1600Ter
NM_001363725.1:c.2548C>T	NP_001350654.1:p.Gln850Ter
XM_011535984.2:c.5008C>T	XP_011534286.2:p.Gln1670Ter
XM_011535988.3:c.1939C>T	XP_011534290.1:p.Gln647Ter
XM_017011103.2:c.4909C>T	XP_016866592.1:p.Gln1637Ter
XM_017011104.1:c.4879C>T	XP_016866593.1:p.Gln1627Ter
XM_017011105.2:c.4849C>T	XP_016866594.1:p.Gln1617Ter
XM_017011106.2:c.4720C>T	XP_016866595.1:p.Gln1574Ter
XM_017011107.2:c.4699C>T	XP_016866596.1:p.Gln1567Ter
XR_002956289.1:n.4994C>T
NM_001363725.2:c.2548C>T	NP_001350654.1:p.Gln850Ter
NM_001371656.1:c.4927C>T	NP_001358585.1:p.Gln1643Ter
NM_001374820.1:c.4927C>T	NP_001361749.1:p.Gln1643Ter
NM_001374828.1:c.5047C>T MANE Select	NP_001361757.1:p.Gln1683Ter
NM_017519.3:c.4888C>T	NP_059989.3:p.Gln1630Ter