Canonical Allele Identifier: CA366240908

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1679391
• ClinVar RCV Id: RCV002226988 ; RCV003718450
• dbSNP Id: rs1554235541
• MyVariant Identifiers: chr6:g.157521911C>T (hg19) ; chr6:g.157200777C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200777C>T , CM000668.2:g.157200777C>T	GRCh38
NC_000006.11:g.157521911C>T , CM000668.1:g.157521911C>T	GRCh37
NC_000006.10:g.157563603C>T	NCBI36
NG_032093.1:g.427848C>T
NG_032093.2:g.427848C>T
NG_066624.1:g.429752C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4393C>T	ENSP00000055163.8:p.Gln1465Ter
ENST00000414678.8:c.4462C>T	ENSP00000412835.3:p.Gln1488Ter
ENST00000637015.2:c.4681C>T	ENSP00000489729.2:p.Gln1561Ter
ENST00000346085.10:c.4432C>T	ENSP00000344546.5:p.Gln1478Ter
ENST00000350026.10:c.4144C>T	ENSP00000055163.7:p.Gln1382Ter
ENST00000414678.7:c.2710C>T	ENSP00000412835.2:p.Gln904Ter
ENST00000635849.1:c.1873C>T	ENSP00000490948.1:p.Gln625Ter
ENST00000635957.1:c.1504C>T	ENSP00000490385.1:p.Gln502Ter
ENST00000636227.1:n.3015C>T
ENST00000636254.1:n.472C>T
ENST00000636930.2:c.4552C>T MANE Select	ENSP00000490491.2:p.Gln1518Ter
ENST00000636940.1:n.2549C>T
ENST00000637015.1:c.1920C>T
ENST00000637568.1:c.1834C>T
ENST00000637741.1:n.1218C>T
ENST00000637810.1:c.1894C>T	ENSP00000489636.1:p.Gln632Ter
ENST00000637904.1:c.2053C>T	ENSP00000490550.1:p.Gln685Ter
ENST00000647938.1:c.4183C>T	ENSP00000498155.1:p.Gln1395Ter
ENST00000346085.9:c.4183C>T	ENSP00000344546.4:p.Gln1395Ter
ENST00000350026.9:c.4144C>T	ENSP00000055163.7:p.Gln1382Ter
ENST00000414678.6:c.2710C>T	ENSP00000412835.2:p.Gln904Ter
NM_017519.2:c.4144C>T	NP_059989.2:p.Gln1382Ter
NM_020732.3:c.4183C>T	NP_065783.3:p.Gln1395Ter
XM_005267069.3:c.4303C>T	XP_005267126.2:p.Gln1435Ter
XM_011535984.1:c.3382C>T	XP_011534286.1:p.Gln1128Ter
XM_011535985.1:c.3202C>T	XP_011534287.1:p.Gln1068Ter
XM_011535986.1:c.2962C>T	XP_011534288.1:p.Gln988Ter
XM_011535987.1:c.2581C>T	XP_011534289.1:p.Gln861Ter
XM_011535988.1:c.1444C>T	XP_011534290.1:p.Gln482Ter
NM_001346813.1:c.4303C>T	NP_001333742.1:p.Gln1435Ter
NM_001363725.1:c.2053C>T	NP_001350654.1:p.Gln685Ter
XM_011535984.2:c.4513C>T	XP_011534286.2:p.Gln1505Ter
XM_011535988.3:c.1444C>T	XP_011534290.1:p.Gln482Ter
XM_017011103.2:c.4414C>T	XP_016866592.1:p.Gln1472Ter
XM_017011104.1:c.4384C>T	XP_016866593.1:p.Gln1462Ter
XM_017011105.2:c.4354C>T	XP_016866594.1:p.Gln1452Ter
XM_017011106.2:c.4225C>T	XP_016866595.1:p.Gln1409Ter
XM_017011107.2:c.4204C>T	XP_016866596.1:p.Gln1402Ter
XR_002956289.1:n.4499C>T
NM_001363725.2:c.2053C>T	NP_001350654.1:p.Gln685Ter
NM_001371656.1:c.4432C>T	NP_001358585.1:p.Gln1478Ter
NM_001374820.1:c.4432C>T	NP_001361749.1:p.Gln1478Ter
NM_001374828.1:c.4552C>T MANE Select	NP_001361757.1:p.Gln1518Ter
NM_017519.3:c.4393C>T	NP_059989.3:p.Gln1465Ter