Canonical Allele Identifier: CA366234167

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128338921
• MyVariant Identifiers: chr6:g.157510858G>C (hg19) ; chr6:g.157189724G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189724G>C , CM000668.2:g.157189724G>C	GRCh38
NC_000006.11:g.157510858G>C , CM000668.1:g.157510858G>C	GRCh37
NC_000006.10:g.157552550G>C	NCBI36
NG_032093.1:g.416795G>C
NG_032093.2:g.416795G>C
NG_066624.1:g.418699G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3843G>C	ENSP00000055163.8:p.Lys1281Asn
ENST00000414678.8:c.3912G>C	ENSP00000412835.3:p.Lys1304Asn
ENST00000637015.2:c.4131G>C	ENSP00000489729.2:p.Lys1377Asn
ENST00000346085.10:c.3882G>C	ENSP00000344546.5:p.Lys1294Asn
ENST00000350026.10:c.3594G>C	ENSP00000055163.7:p.Lys1198Asn
ENST00000414678.7:c.2160G>C	ENSP00000412835.2:p.Lys720Asn
ENST00000635849.1:c.1323G>C	ENSP00000490948.1:p.Lys441Asn
ENST00000635957.1:c.957G>C	ENSP00000490385.1:p.Lys319Asn
ENST00000636930.2:c.4002G>C MANE Select	ENSP00000490491.2:p.Lys1334Asn
ENST00000636940.1:n.1999G>C
ENST00000637015.1:c.1370G>C
ENST00000637568.1:c.1284G>C
ENST00000637741.1:n.668G>C
ENST00000637810.1:c.1344G>C	ENSP00000489636.1:p.Lys448Asn
ENST00000637904.1:c.1503G>C	ENSP00000490550.1:p.Lys501Asn
ENST00000647938.1:c.3633G>C	ENSP00000498155.1:p.Lys1211Asn
ENST00000346085.9:c.3633G>C	ENSP00000344546.4:p.Lys1211Asn
ENST00000350026.9:c.3594G>C	ENSP00000055163.7:p.Lys1198Asn
ENST00000414678.6:c.2160G>C	ENSP00000412835.2:p.Lys720Asn
NM_017519.2:c.3594G>C	NP_059989.2:p.Lys1198Asn
NM_020732.3:c.3633G>C	NP_065783.3:p.Lys1211Asn
XM_005267069.3:c.3753G>C	XP_005267126.2:p.Lys1251Asn
XM_011535984.1:c.2832G>C	XP_011534286.1:p.Lys944Asn
XM_011535985.1:c.2652G>C	XP_011534287.1:p.Lys884Asn
XM_011535986.1:c.2412G>C	XP_011534288.1:p.Lys804Asn
XM_011535987.1:c.2031G>C	XP_011534289.1:p.Lys677Asn
XM_011535988.1:c.894G>C	XP_011534290.1:p.Lys298Asn
NM_001346813.1:c.3753G>C	NP_001333742.1:p.Lys1251Asn
NM_001363725.1:c.1503G>C	NP_001350654.1:p.Lys501Asn
XM_011535984.2:c.3963G>C	XP_011534286.2:p.Lys1321Asn
XM_011535988.3:c.894G>C	XP_011534290.1:p.Lys298Asn
XM_017011103.2:c.3864G>C	XP_016866592.1:p.Lys1288Asn
XM_017011104.1:c.3834G>C	XP_016866593.1:p.Lys1278Asn
XM_017011105.2:c.3804G>C	XP_016866594.1:p.Lys1268Asn
XM_017011106.2:c.3675G>C	XP_016866595.1:p.Lys1225Asn
XM_017011107.2:c.3654G>C	XP_016866596.1:p.Lys1218Asn
XR_002956289.1:n.4046G>C
NM_001363725.2:c.1503G>C	NP_001350654.1:p.Lys501Asn
NM_001371656.1:c.3882G>C	NP_001358585.1:p.Lys1294Asn
NM_001374820.1:c.3882G>C	NP_001361749.1:p.Lys1294Asn
NM_001374828.1:c.4002G>C MANE Select	NP_001361757.1:p.Lys1334Asn
NM_017519.3:c.3843G>C	NP_059989.3:p.Lys1281Asn