Canonical Allele Identifier: CA358558

Gene: ARID1B

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207241C>T , CM000668.2:g.157207241C>T	GRCh38
NC_000006.11:g.157528375C>T , CM000668.1:g.157528375C>T	GRCh37
NC_000006.10:g.157570067C>T	NCBI36
NG_032093.1:g.434312C>T
NG_032093.2:g.434312C>T
NG_066624.1:g.436216C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.6310C>T	ENSP00000055163.8:p.Gln2104Ter
ENST00000414678.8:c.6379C>T	ENSP00000412835.3:p.Gln2127Ter
ENST00000637015.2:c.6598C>T	ENSP00000489729.2:p.Gln2200Ter
ENST00000346085.10:c.6349C>T	ENSP00000344546.5:p.Gln2117Ter
ENST00000350026.10:c.6061C>T	ENSP00000055163.7:p.Gln2021Ter
ENST00000414678.7:c.4627C>T	ENSP00000412835.2:p.Gln1543Ter
ENST00000635849.1:c.3790C>T	ENSP00000490948.1:p.Gln1264Ter
ENST00000635928.1:c.625C>T	ENSP00000489717.1:p.Gln209Ter
ENST00000635957.1:c.3421C>T	ENSP00000490385.1:p.Gln1141Ter
ENST00000636227.1:n.4932C>T
ENST00000636254.1:n.2389C>T
ENST00000636930.2:c.6469C>T MANE Select	ENSP00000490491.2:p.Gln2157Ter
ENST00000636940.1:n.4466C>T
ENST00000637015.1:c.3837C>T
ENST00000637568.1:c.3751C>T
ENST00000637741.1:n.3135C>T
ENST00000637810.1:c.3811C>T	ENSP00000489636.1:p.Gln1271Ter
ENST00000637904.1:c.3970C>T	ENSP00000490550.1:p.Gln1324Ter
ENST00000637933.1:n.3584C>T
ENST00000647938.1:c.6100C>T	ENSP00000498155.1:p.Gln2034Ter
ENST00000346085.9:c.6100C>T	ENSP00000344546.4:p.Gln2034Ter
ENST00000350026.9:c.6061C>T	ENSP00000055163.7:p.Gln2021Ter
ENST00000414678.6:c.4627C>T	ENSP00000412835.2:p.Gln1543Ter
NM_017519.2:c.6061C>T	NP_059989.2:p.Gln2021Ter
NM_020732.3:c.6100C>T	NP_065783.3:p.Gln2034Ter
XM_005267069.3:c.6220C>T	XP_005267126.2:p.Gln2074Ter
XM_011535984.1:c.5299C>T	XP_011534286.1:p.Gln1767Ter
XM_011535985.1:c.5119C>T	XP_011534287.1:p.Gln1707Ter
XM_011535986.1:c.4879C>T	XP_011534288.1:p.Gln1627Ter
XM_011535987.1:c.4498C>T	XP_011534289.1:p.Gln1500Ter
XM_011535988.1:c.3361C>T	XP_011534290.1:p.Gln1121Ter
NM_001346813.1:c.6220C>T	NP_001333742.1:p.Gln2074Ter
NM_001363725.1:c.3970C>T	NP_001350654.1:p.Gln1324Ter
XM_011535984.2:c.6430C>T	XP_011534286.2:p.Gln2144Ter
XM_011535988.3:c.3361C>T	XP_011534290.1:p.Gln1121Ter
XM_017011103.2:c.6331C>T	XP_016866592.1:p.Gln2111Ter
XM_017011104.1:c.6301C>T	XP_016866593.1:p.Gln2101Ter
XM_017011105.2:c.6271C>T	XP_016866594.1:p.Gln2091Ter
XM_017011106.2:c.6142C>T	XP_016866595.1:p.Gln2048Ter
XM_017011107.2:c.6121C>T	XP_016866596.1:p.Gln2041Ter
XR_002956289.1:n.6416C>T
NM_001363725.2:c.3970C>T	NP_001350654.1:p.Gln1324Ter
NM_001371656.1:c.6349C>T	NP_001358585.1:p.Gln2117Ter
NM_001374820.1:c.6349C>T	NP_001361749.1:p.Gln2117Ter
NM_001374828.1:c.6469C>T MANE Select	NP_001361757.1:p.Gln2157Ter
NM_017519.3:c.6310C>T	NP_059989.3:p.Gln2104Ter