Canonical Allele Identifier: CA366234048

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 845891
• ClinVar RCV Id: RCV001049055 ; RCV002272397
• dbSNP Id: rs1554232925
• MyVariant Identifiers: chr6:g.157510802C>T (hg19) ; chr6:g.157189668C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189668C>T , CM000668.2:g.157189668C>T	GRCh38
NC_000006.11:g.157510802C>T , CM000668.1:g.157510802C>T	GRCh37
NC_000006.10:g.157552494C>T	NCBI36
NG_032093.1:g.416739C>T
NG_032093.2:g.416739C>T
NG_066624.1:g.418643C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3787C>T	ENSP00000055163.8:p.Gln1263Ter
ENST00000414678.8:c.3856C>T	ENSP00000412835.3:p.Gln1286Ter
ENST00000637015.2:c.4075C>T	ENSP00000489729.2:p.Gln1359Ter
ENST00000346085.10:c.3826C>T	ENSP00000344546.5:p.Gln1276Ter
ENST00000350026.10:c.3538C>T	ENSP00000055163.7:p.Gln1180Ter
ENST00000414678.7:c.2104C>T	ENSP00000412835.2:p.Gln702Ter
ENST00000635849.1:c.1267C>T	ENSP00000490948.1:p.Gln423Ter
ENST00000635957.1:c.901C>T	ENSP00000490385.1:p.Gln301Ter
ENST00000636930.2:c.3946C>T MANE Select	ENSP00000490491.2:p.Gln1316Ter
ENST00000636940.1:n.1943C>T
ENST00000637015.1:c.1314C>T
ENST00000637568.1:c.1228C>T
ENST00000637741.1:n.612C>T
ENST00000637810.1:c.1288C>T	ENSP00000489636.1:p.Gln430Ter
ENST00000637904.1:c.1447C>T	ENSP00000490550.1:p.Gln483Ter
ENST00000647938.1:c.3577C>T	ENSP00000498155.1:p.Gln1193Ter
ENST00000346085.9:c.3577C>T	ENSP00000344546.4:p.Gln1193Ter
ENST00000350026.9:c.3538C>T	ENSP00000055163.7:p.Gln1180Ter
ENST00000414678.6:c.2104C>T	ENSP00000412835.2:p.Gln702Ter
NM_017519.2:c.3538C>T	NP_059989.2:p.Gln1180Ter
NM_020732.3:c.3577C>T	NP_065783.3:p.Gln1193Ter
XM_005267069.3:c.3697C>T	XP_005267126.2:p.Gln1233Ter
XM_011535984.1:c.2776C>T	XP_011534286.1:p.Gln926Ter
XM_011535985.1:c.2596C>T	XP_011534287.1:p.Gln866Ter
XM_011535986.1:c.2356C>T	XP_011534288.1:p.Gln786Ter
XM_011535987.1:c.1975C>T	XP_011534289.1:p.Gln659Ter
XM_011535988.1:c.838C>T	XP_011534290.1:p.Gln280Ter
NM_001346813.1:c.3697C>T	NP_001333742.1:p.Gln1233Ter
NM_001363725.1:c.1447C>T	NP_001350654.1:p.Gln483Ter
XM_011535984.2:c.3907C>T	XP_011534286.2:p.Gln1303Ter
XM_011535988.3:c.838C>T	XP_011534290.1:p.Gln280Ter
XM_017011103.2:c.3808C>T	XP_016866592.1:p.Gln1270Ter
XM_017011104.1:c.3778C>T	XP_016866593.1:p.Gln1260Ter
XM_017011105.2:c.3748C>T	XP_016866594.1:p.Gln1250Ter
XM_017011106.2:c.3619C>T	XP_016866595.1:p.Gln1207Ter
XM_017011107.2:c.3598C>T	XP_016866596.1:p.Gln1200Ter
XR_002956289.1:n.3990C>T
NM_001363725.2:c.1447C>T	NP_001350654.1:p.Gln483Ter
NM_001371656.1:c.3826C>T	NP_001358585.1:p.Gln1276Ter
NM_001374820.1:c.3826C>T	NP_001361749.1:p.Gln1276Ter
NM_001374828.1:c.3946C>T MANE Select	NP_001361757.1:p.Gln1316Ter
NM_017519.3:c.3787C>T	NP_059989.3:p.Gln1263Ter