Canonical Allele Identifier: CA366241538

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2062420
• ClinVar RCV Id: RCV002957709
• MyVariant Identifiers: chr6:g.157522154C>T (hg19) ; chr6:g.157201020C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201020C>T , CM000668.2:g.157201020C>T	GRCh38
NC_000006.11:g.157522154C>T , CM000668.1:g.157522154C>T	GRCh37
NC_000006.10:g.157563846C>T	NCBI36
NG_032093.1:g.428091C>T
NG_032093.2:g.428091C>T
NG_066624.1:g.429995C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4636C>T	ENSP00000055163.8:p.Gln1546Ter
ENST00000414678.8:c.4705C>T	ENSP00000412835.3:p.Gln1569Ter
ENST00000637015.2:c.4924C>T	ENSP00000489729.2:p.Gln1642Ter
ENST00000346085.10:c.4675C>T	ENSP00000344546.5:p.Gln1559Ter
ENST00000350026.10:c.4387C>T	ENSP00000055163.7:p.Gln1463Ter
ENST00000414678.7:c.2953C>T	ENSP00000412835.2:p.Gln985Ter
ENST00000635849.1:c.2116C>T	ENSP00000490948.1:p.Gln706Ter
ENST00000635957.1:c.1747C>T	ENSP00000490385.1:p.Gln583Ter
ENST00000636227.1:n.3258C>T
ENST00000636254.1:n.715C>T
ENST00000636930.2:c.4795C>T MANE Select	ENSP00000490491.2:p.Gln1599Ter
ENST00000636940.1:n.2792C>T
ENST00000637015.1:c.2163C>T
ENST00000637568.1:c.2077C>T
ENST00000637741.1:n.1461C>T
ENST00000637810.1:c.2137C>T	ENSP00000489636.1:p.Gln713Ter
ENST00000637904.1:c.2296C>T	ENSP00000490550.1:p.Gln766Ter
ENST00000647938.1:c.4426C>T	ENSP00000498155.1:p.Gln1476Ter
ENST00000346085.9:c.4426C>T	ENSP00000344546.4:p.Gln1476Ter
ENST00000350026.9:c.4387C>T	ENSP00000055163.7:p.Gln1463Ter
ENST00000414678.6:c.2953C>T	ENSP00000412835.2:p.Gln985Ter
NM_017519.2:c.4387C>T	NP_059989.2:p.Gln1463Ter
NM_020732.3:c.4426C>T	NP_065783.3:p.Gln1476Ter
XM_005267069.3:c.4546C>T	XP_005267126.2:p.Gln1516Ter
XM_011535984.1:c.3625C>T	XP_011534286.1:p.Gln1209Ter
XM_011535985.1:c.3445C>T	XP_011534287.1:p.Gln1149Ter
XM_011535986.1:c.3205C>T	XP_011534288.1:p.Gln1069Ter
XM_011535987.1:c.2824C>T	XP_011534289.1:p.Gln942Ter
XM_011535988.1:c.1687C>T	XP_011534290.1:p.Gln563Ter
NM_001346813.1:c.4546C>T	NP_001333742.1:p.Gln1516Ter
NM_001363725.1:c.2296C>T	NP_001350654.1:p.Gln766Ter
XM_011535984.2:c.4756C>T	XP_011534286.2:p.Gln1586Ter
XM_011535988.3:c.1687C>T	XP_011534290.1:p.Gln563Ter
XM_017011103.2:c.4657C>T	XP_016866592.1:p.Gln1553Ter
XM_017011104.1:c.4627C>T	XP_016866593.1:p.Gln1543Ter
XM_017011105.2:c.4597C>T	XP_016866594.1:p.Gln1533Ter
XM_017011106.2:c.4468C>T	XP_016866595.1:p.Gln1490Ter
XM_017011107.2:c.4447C>T	XP_016866596.1:p.Gln1483Ter
XR_002956289.1:n.4742C>T
NM_001363725.2:c.2296C>T	NP_001350654.1:p.Gln766Ter
NM_001371656.1:c.4675C>T	NP_001358585.1:p.Gln1559Ter
NM_001374820.1:c.4675C>T	NP_001361749.1:p.Gln1559Ter
NM_001374828.1:c.4795C>T MANE Select	NP_001361757.1:p.Gln1599Ter
NM_017519.3:c.4636C>T	NP_059989.3:p.Gln1546Ter