Canonical Allele Identifier: CA366234682

Gene: ARID1B

Linked Data

• dbSNP Id: rs1793245423
• MyVariant Identifiers: chr6:g.157511183T>C (hg19) ; chr6:g.157190049T>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3911T>C	ENSP00000055163.8:p.Ile1304Thr
ENST00000414678.8:c.3980T>C	ENSP00000412835.3:p.Ile1327Thr
ENST00000637015.2:c.4199T>C	ENSP00000489729.2:p.Ile1400Thr
ENST00000346085.10:c.3950T>C	ENSP00000344546.5:p.Ile1317Thr
ENST00000350026.10:c.3662T>C	ENSP00000055163.7:p.Ile1221Thr
ENST00000414678.7:c.2228T>C	ENSP00000412835.2:p.Ile743Thr
ENST00000635849.1:c.1391T>C	ENSP00000490948.1:p.Ile464Thr
ENST00000635957.1:c.1022T>C	ENSP00000490385.1:p.Ile341Thr
ENST00000636930.2:c.4070T>C MANE Select	ENSP00000490491.2:p.Ile1357Thr
ENST00000636940.1:n.2067T>C
ENST00000637015.1:c.1438T>C
ENST00000637568.1:c.1352T>C
ENST00000637741.1:n.736T>C
ENST00000637810.1:c.1412T>C	ENSP00000489636.1:p.Ile471Thr
ENST00000637904.1:c.1571T>C	ENSP00000490550.1:p.Ile524Thr
ENST00000647938.1:c.3701T>C	ENSP00000498155.1:p.Ile1234Thr
ENST00000346085.9:c.3701T>C	ENSP00000344546.4:p.Ile1234Thr
ENST00000350026.9:c.3662T>C	ENSP00000055163.7:p.Ile1221Thr
ENST00000414678.6:c.2228T>C	ENSP00000412835.2:p.Ile743Thr
NM_017519.2:c.3662T>C	NP_059989.2:p.Ile1221Thr
NM_020732.3:c.3701T>C	NP_065783.3:p.Ile1234Thr
XM_005267069.3:c.3821T>C	XP_005267126.2:p.Ile1274Thr
XM_011535984.1:c.2900T>C	XP_011534286.1:p.Ile967Thr
XM_011535985.1:c.2720T>C	XP_011534287.1:p.Ile907Thr
XM_011535986.1:c.2480T>C	XP_011534288.1:p.Ile827Thr
XM_011535987.1:c.2099T>C	XP_011534289.1:p.Ile700Thr
XM_011535988.1:c.962T>C	XP_011534290.1:p.Ile321Thr
NM_001346813.1:c.3821T>C	NP_001333742.1:p.Ile1274Thr
NM_001363725.1:c.1571T>C	NP_001350654.1:p.Ile524Thr
XM_011535984.2:c.4031T>C	XP_011534286.2:p.Ile1344Thr
XM_011535988.3:c.962T>C	XP_011534290.1:p.Ile321Thr
XM_017011103.2:c.3932T>C	XP_016866592.1:p.Ile1311Thr
XM_017011104.1:c.3902T>C	XP_016866593.1:p.Ile1301Thr
XM_017011105.2:c.3872T>C	XP_016866594.1:p.Ile1291Thr
XM_017011106.2:c.3743T>C	XP_016866595.1:p.Ile1248Thr
XM_017011107.2:c.3722T>C	XP_016866596.1:p.Ile1241Thr
XR_002956289.1:n.4114T>C
NM_001363725.2:c.1571T>C	NP_001350654.1:p.Ile524Thr
NM_001371656.1:c.3950T>C	NP_001358585.1:p.Ile1317Thr
NM_001374820.1:c.3950T>C	NP_001361749.1:p.Ile1317Thr
NM_001374828.1:c.4070T>C MANE Select	NP_001361757.1:p.Ile1357Thr
NM_017519.3:c.3911T>C	NP_059989.3:p.Ile1304Thr