Canonical Allele Identifier: CA366234679

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511183T>A (hg19) ; chr6:g.157190049T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190049T>A , CM000668.2:g.157190049T>A	GRCh38
NC_000006.11:g.157511183T>A , CM000668.1:g.157511183T>A	GRCh37
NC_000006.10:g.157552875T>A	NCBI36
NG_032093.1:g.417120T>A
NG_032093.2:g.417120T>A
NG_066624.1:g.419024T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3911T>A	ENSP00000055163.8:p.Ile1304Asn
ENST00000414678.8:c.3980T>A	ENSP00000412835.3:p.Ile1327Asn
ENST00000637015.2:c.4199T>A	ENSP00000489729.2:p.Ile1400Asn
ENST00000346085.10:c.3950T>A	ENSP00000344546.5:p.Ile1317Asn
ENST00000350026.10:c.3662T>A	ENSP00000055163.7:p.Ile1221Asn
ENST00000414678.7:c.2228T>A	ENSP00000412835.2:p.Ile743Asn
ENST00000635849.1:c.1391T>A	ENSP00000490948.1:p.Ile464Asn
ENST00000635957.1:c.1022T>A	ENSP00000490385.1:p.Ile341Asn
ENST00000636930.2:c.4070T>A MANE Select	ENSP00000490491.2:p.Ile1357Asn
ENST00000636940.1:n.2067T>A
ENST00000637015.1:c.1438T>A
ENST00000637568.1:c.1352T>A
ENST00000637741.1:n.736T>A
ENST00000637810.1:c.1412T>A	ENSP00000489636.1:p.Ile471Asn
ENST00000637904.1:c.1571T>A	ENSP00000490550.1:p.Ile524Asn
ENST00000647938.1:c.3701T>A	ENSP00000498155.1:p.Ile1234Asn
ENST00000346085.9:c.3701T>A	ENSP00000344546.4:p.Ile1234Asn
ENST00000350026.9:c.3662T>A	ENSP00000055163.7:p.Ile1221Asn
ENST00000414678.6:c.2228T>A	ENSP00000412835.2:p.Ile743Asn
NM_017519.2:c.3662T>A	NP_059989.2:p.Ile1221Asn
NM_020732.3:c.3701T>A	NP_065783.3:p.Ile1234Asn
XM_005267069.3:c.3821T>A	XP_005267126.2:p.Ile1274Asn
XM_011535984.1:c.2900T>A	XP_011534286.1:p.Ile967Asn
XM_011535985.1:c.2720T>A	XP_011534287.1:p.Ile907Asn
XM_011535986.1:c.2480T>A	XP_011534288.1:p.Ile827Asn
XM_011535987.1:c.2099T>A	XP_011534289.1:p.Ile700Asn
XM_011535988.1:c.962T>A	XP_011534290.1:p.Ile321Asn
NM_001346813.1:c.3821T>A	NP_001333742.1:p.Ile1274Asn
NM_001363725.1:c.1571T>A	NP_001350654.1:p.Ile524Asn
XM_011535984.2:c.4031T>A	XP_011534286.2:p.Ile1344Asn
XM_011535988.3:c.962T>A	XP_011534290.1:p.Ile321Asn
XM_017011103.2:c.3932T>A	XP_016866592.1:p.Ile1311Asn
XM_017011104.1:c.3902T>A	XP_016866593.1:p.Ile1301Asn
XM_017011105.2:c.3872T>A	XP_016866594.1:p.Ile1291Asn
XM_017011106.2:c.3743T>A	XP_016866595.1:p.Ile1248Asn
XM_017011107.2:c.3722T>A	XP_016866596.1:p.Ile1241Asn
XR_002956289.1:n.4114T>A
NM_001363725.2:c.1571T>A	NP_001350654.1:p.Ile524Asn
NM_001371656.1:c.3950T>A	NP_001358585.1:p.Ile1317Asn
NM_001374820.1:c.3950T>A	NP_001361749.1:p.Ile1317Asn
NM_001374828.1:c.4070T>A MANE Select	NP_001361757.1:p.Ile1357Asn
NM_017519.3:c.3911T>A	NP_059989.3:p.Ile1304Asn