Canonical Allele Identifier: CA366234164

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510857A>C (hg19) ; chr6:g.157189723A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189723A>C , CM000668.2:g.157189723A>C	GRCh38
NC_000006.11:g.157510857A>C , CM000668.1:g.157510857A>C	GRCh37
NC_000006.10:g.157552549A>C	NCBI36
NG_032093.1:g.416794A>C
NG_032093.2:g.416794A>C
NG_066624.1:g.418698A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3842A>C	ENSP00000055163.8:p.Lys1281Thr
ENST00000414678.8:c.3911A>C	ENSP00000412835.3:p.Lys1304Thr
ENST00000637015.2:c.4130A>C	ENSP00000489729.2:p.Lys1377Thr
ENST00000346085.10:c.3881A>C	ENSP00000344546.5:p.Lys1294Thr
ENST00000350026.10:c.3593A>C	ENSP00000055163.7:p.Lys1198Thr
ENST00000414678.7:c.2159A>C	ENSP00000412835.2:p.Lys720Thr
ENST00000635849.1:c.1322A>C	ENSP00000490948.1:p.Lys441Thr
ENST00000635957.1:c.956A>C	ENSP00000490385.1:p.Lys319Thr
ENST00000636930.2:c.4001A>C MANE Select	ENSP00000490491.2:p.Lys1334Thr
ENST00000636940.1:n.1998A>C
ENST00000637015.1:c.1369A>C
ENST00000637568.1:c.1283A>C
ENST00000637741.1:n.667A>C
ENST00000637810.1:c.1343A>C	ENSP00000489636.1:p.Lys448Thr
ENST00000637904.1:c.1502A>C	ENSP00000490550.1:p.Lys501Thr
ENST00000647938.1:c.3632A>C	ENSP00000498155.1:p.Lys1211Thr
ENST00000346085.9:c.3632A>C	ENSP00000344546.4:p.Lys1211Thr
ENST00000350026.9:c.3593A>C	ENSP00000055163.7:p.Lys1198Thr
ENST00000414678.6:c.2159A>C	ENSP00000412835.2:p.Lys720Thr
NM_017519.2:c.3593A>C	NP_059989.2:p.Lys1198Thr
NM_020732.3:c.3632A>C	NP_065783.3:p.Lys1211Thr
XM_005267069.3:c.3752A>C	XP_005267126.2:p.Lys1251Thr
XM_011535984.1:c.2831A>C	XP_011534286.1:p.Lys944Thr
XM_011535985.1:c.2651A>C	XP_011534287.1:p.Lys884Thr
XM_011535986.1:c.2411A>C	XP_011534288.1:p.Lys804Thr
XM_011535987.1:c.2030A>C	XP_011534289.1:p.Lys677Thr
XM_011535988.1:c.893A>C	XP_011534290.1:p.Lys298Thr
NM_001346813.1:c.3752A>C	NP_001333742.1:p.Lys1251Thr
NM_001363725.1:c.1502A>C	NP_001350654.1:p.Lys501Thr
XM_011535984.2:c.3962A>C	XP_011534286.2:p.Lys1321Thr
XM_011535988.3:c.893A>C	XP_011534290.1:p.Lys298Thr
XM_017011103.2:c.3863A>C	XP_016866592.1:p.Lys1288Thr
XM_017011104.1:c.3833A>C	XP_016866593.1:p.Lys1278Thr
XM_017011105.2:c.3803A>C	XP_016866594.1:p.Lys1268Thr
XM_017011106.2:c.3674A>C	XP_016866595.1:p.Lys1225Thr
XM_017011107.2:c.3653A>C	XP_016866596.1:p.Lys1218Thr
XR_002956289.1:n.4045A>C
NM_001363725.2:c.1502A>C	NP_001350654.1:p.Lys501Thr
NM_001371656.1:c.3881A>C	NP_001358585.1:p.Lys1294Thr
NM_001374820.1:c.3881A>C	NP_001361749.1:p.Lys1294Thr
NM_001374828.1:c.4001A>C MANE Select	NP_001361757.1:p.Lys1334Thr
NM_017519.3:c.3842A>C	NP_059989.3:p.Lys1281Thr