Canonical Allele Identifier: CA366234684

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3911T>G	ENSP00000055163.8:p.Ile1304Ser
ENST00000414678.8:c.3980T>G	ENSP00000412835.3:p.Ile1327Ser
ENST00000637015.2:c.4199T>G	ENSP00000489729.2:p.Ile1400Ser
ENST00000346085.10:c.3950T>G	ENSP00000344546.5:p.Ile1317Ser
ENST00000350026.10:c.3662T>G	ENSP00000055163.7:p.Ile1221Ser
ENST00000414678.7:c.2228T>G	ENSP00000412835.2:p.Ile743Ser
ENST00000635849.1:c.1391T>G	ENSP00000490948.1:p.Ile464Ser
ENST00000635957.1:c.1022T>G	ENSP00000490385.1:p.Ile341Ser
ENST00000636930.2:c.4070T>G MANE Select	ENSP00000490491.2:p.Ile1357Ser
ENST00000636940.1:n.2067T>G
ENST00000637015.1:c.1438T>G
ENST00000637568.1:c.1352T>G
ENST00000637741.1:n.736T>G
ENST00000637810.1:c.1412T>G	ENSP00000489636.1:p.Ile471Ser
ENST00000637904.1:c.1571T>G	ENSP00000490550.1:p.Ile524Ser
ENST00000647938.1:c.3701T>G	ENSP00000498155.1:p.Ile1234Ser
ENST00000346085.9:c.3701T>G	ENSP00000344546.4:p.Ile1234Ser
ENST00000350026.9:c.3662T>G	ENSP00000055163.7:p.Ile1221Ser
ENST00000414678.6:c.2228T>G	ENSP00000412835.2:p.Ile743Ser
NM_017519.2:c.3662T>G	NP_059989.2:p.Ile1221Ser
NM_020732.3:c.3701T>G	NP_065783.3:p.Ile1234Ser
XM_005267069.3:c.3821T>G	XP_005267126.2:p.Ile1274Ser
XM_011535984.1:c.2900T>G	XP_011534286.1:p.Ile967Ser
XM_011535985.1:c.2720T>G	XP_011534287.1:p.Ile907Ser
XM_011535986.1:c.2480T>G	XP_011534288.1:p.Ile827Ser
XM_011535987.1:c.2099T>G	XP_011534289.1:p.Ile700Ser
XM_011535988.1:c.962T>G	XP_011534290.1:p.Ile321Ser
NM_001346813.1:c.3821T>G	NP_001333742.1:p.Ile1274Ser
NM_001363725.1:c.1571T>G	NP_001350654.1:p.Ile524Ser
XM_011535984.2:c.4031T>G	XP_011534286.2:p.Ile1344Ser
XM_011535988.3:c.962T>G	XP_011534290.1:p.Ile321Ser
XM_017011103.2:c.3932T>G	XP_016866592.1:p.Ile1311Ser
XM_017011104.1:c.3902T>G	XP_016866593.1:p.Ile1301Ser
XM_017011105.2:c.3872T>G	XP_016866594.1:p.Ile1291Ser
XM_017011106.2:c.3743T>G	XP_016866595.1:p.Ile1248Ser
XM_017011107.2:c.3722T>G	XP_016866596.1:p.Ile1241Ser
XR_002956289.1:n.4114T>G
NM_001363725.2:c.1571T>G	NP_001350654.1:p.Ile524Ser
NM_001371656.1:c.3950T>G	NP_001358585.1:p.Ile1317Ser
NM_001374820.1:c.3950T>G	NP_001361749.1:p.Ile1317Ser
NM_001374828.1:c.4070T>G MANE Select	NP_001361757.1:p.Ile1357Ser
NM_017519.3:c.3911T>G	NP_059989.3:p.Ile1304Ser