Canonical Allele Identifier: CA366234161

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510856A>C (hg19) ; chr6:g.157189722A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189722A>C , CM000668.2:g.157189722A>C	GRCh38
NC_000006.11:g.157510856A>C , CM000668.1:g.157510856A>C	GRCh37
NC_000006.10:g.157552548A>C	NCBI36
NG_032093.1:g.416793A>C
NG_032093.2:g.416793A>C
NG_066624.1:g.418697A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3841A>C	ENSP00000055163.8:p.Lys1281Gln
ENST00000414678.8:c.3910A>C	ENSP00000412835.3:p.Lys1304Gln
ENST00000637015.2:c.4129A>C	ENSP00000489729.2:p.Lys1377Gln
ENST00000346085.10:c.3880A>C	ENSP00000344546.5:p.Lys1294Gln
ENST00000350026.10:c.3592A>C	ENSP00000055163.7:p.Lys1198Gln
ENST00000414678.7:c.2158A>C	ENSP00000412835.2:p.Lys720Gln
ENST00000635849.1:c.1321A>C	ENSP00000490948.1:p.Lys441Gln
ENST00000635957.1:c.955A>C	ENSP00000490385.1:p.Lys319Gln
ENST00000636930.2:c.4000A>C MANE Select	ENSP00000490491.2:p.Lys1334Gln
ENST00000636940.1:n.1997A>C
ENST00000637015.1:c.1368A>C
ENST00000637568.1:c.1282A>C
ENST00000637741.1:n.666A>C
ENST00000637810.1:c.1342A>C	ENSP00000489636.1:p.Lys448Gln
ENST00000637904.1:c.1501A>C	ENSP00000490550.1:p.Lys501Gln
ENST00000647938.1:c.3631A>C	ENSP00000498155.1:p.Lys1211Gln
ENST00000346085.9:c.3631A>C	ENSP00000344546.4:p.Lys1211Gln
ENST00000350026.9:c.3592A>C	ENSP00000055163.7:p.Lys1198Gln
ENST00000414678.6:c.2158A>C	ENSP00000412835.2:p.Lys720Gln
NM_017519.2:c.3592A>C	NP_059989.2:p.Lys1198Gln
NM_020732.3:c.3631A>C	NP_065783.3:p.Lys1211Gln
XM_005267069.3:c.3751A>C	XP_005267126.2:p.Lys1251Gln
XM_011535984.1:c.2830A>C	XP_011534286.1:p.Lys944Gln
XM_011535985.1:c.2650A>C	XP_011534287.1:p.Lys884Gln
XM_011535986.1:c.2410A>C	XP_011534288.1:p.Lys804Gln
XM_011535987.1:c.2029A>C	XP_011534289.1:p.Lys677Gln
XM_011535988.1:c.892A>C	XP_011534290.1:p.Lys298Gln
NM_001346813.1:c.3751A>C	NP_001333742.1:p.Lys1251Gln
NM_001363725.1:c.1501A>C	NP_001350654.1:p.Lys501Gln
XM_011535984.2:c.3961A>C	XP_011534286.2:p.Lys1321Gln
XM_011535988.3:c.892A>C	XP_011534290.1:p.Lys298Gln
XM_017011103.2:c.3862A>C	XP_016866592.1:p.Lys1288Gln
XM_017011104.1:c.3832A>C	XP_016866593.1:p.Lys1278Gln
XM_017011105.2:c.3802A>C	XP_016866594.1:p.Lys1268Gln
XM_017011106.2:c.3673A>C	XP_016866595.1:p.Lys1225Gln
XM_017011107.2:c.3652A>C	XP_016866596.1:p.Lys1218Gln
XR_002956289.1:n.4044A>C
NM_001363725.2:c.1501A>C	NP_001350654.1:p.Lys501Gln
NM_001371656.1:c.3880A>C	NP_001358585.1:p.Lys1294Gln
NM_001374820.1:c.3880A>C	NP_001361749.1:p.Lys1294Gln
NM_001374828.1:c.4000A>C MANE Select	NP_001361757.1:p.Lys1334Gln
NM_017519.3:c.3841A>C	NP_059989.3:p.Lys1281Gln