Canonical Allele Identifier: CA452978364

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376021
• MyVariant Identifiers: chr6:g.157522474G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201340G>A , CM000668.2:g.157201340G>A	GRCh38
NC_000006.11:g.157522474G>A , CM000668.1:g.157522474G>A	GRCh37
NC_000006.10:g.157564166G>A	NCBI36
NG_032093.1:g.428411G>A
NG_032093.2:g.428411G>A
NG_066624.1:g.430315G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4956G>A	ENSP00000055163.8:p.Lys1652=
ENST00000414678.8:c.5025G>A	ENSP00000412835.3:p.Lys1675=
ENST00000637015.2:c.5244G>A	ENSP00000489729.2:p.Lys1748=
ENST00000346085.10:c.4995G>A	ENSP00000344546.5:p.Lys1665=
ENST00000350026.10:c.4707G>A	ENSP00000055163.7:p.Lys1569=
ENST00000414678.7:c.3273G>A	ENSP00000412835.2:p.Lys1091=
ENST00000635849.1:c.2436G>A	ENSP00000490948.1:p.Lys812=
ENST00000635957.1:c.2067G>A	ENSP00000490385.1:p.Lys689=
ENST00000636227.1:n.3578G>A
ENST00000636254.1:n.1035G>A
ENST00000636930.2:c.5115G>A MANE Select	ENSP00000490491.2:p.Lys1705=
ENST00000636940.1:n.3112G>A
ENST00000637015.1:c.2483G>A
ENST00000637568.1:c.2397G>A
ENST00000637741.1:n.1781G>A
ENST00000637810.1:c.2457G>A	ENSP00000489636.1:p.Lys819=
ENST00000637904.1:c.2616G>A	ENSP00000490550.1:p.Lys872=
ENST00000647938.1:c.4746G>A	ENSP00000498155.1:p.Lys1582=
ENST00000346085.9:c.4746G>A	ENSP00000344546.4:p.Lys1582=
ENST00000350026.9:c.4707G>A	ENSP00000055163.7:p.Lys1569=
ENST00000414678.6:c.3273G>A	ENSP00000412835.2:p.Lys1091=
NM_017519.2:c.4707G>A	NP_059989.2:p.Lys1569=
NM_020732.3:c.4746G>A	NP_065783.3:p.Lys1582=
XM_005267069.3:c.4866G>A	XP_005267126.2:p.Lys1622=
XM_011535984.1:c.3945G>A	XP_011534286.1:p.Lys1315=
XM_011535985.1:c.3765G>A	XP_011534287.1:p.Lys1255=
XM_011535986.1:c.3525G>A	XP_011534288.1:p.Lys1175=
XM_011535987.1:c.3144G>A	XP_011534289.1:p.Lys1048=
XM_011535988.1:c.2007G>A	XP_011534290.1:p.Lys669=
NM_001346813.1:c.4866G>A	NP_001333742.1:p.Lys1622=
NM_001363725.1:c.2616G>A	NP_001350654.1:p.Lys872=
XM_011535984.2:c.5076G>A	XP_011534286.2:p.Lys1692=
XM_011535988.3:c.2007G>A	XP_011534290.1:p.Lys669=
XM_017011103.2:c.4977G>A	XP_016866592.1:p.Lys1659=
XM_017011104.1:c.4947G>A	XP_016866593.1:p.Lys1649=
XM_017011105.2:c.4917G>A	XP_016866594.1:p.Lys1639=
XM_017011106.2:c.4788G>A	XP_016866595.1:p.Lys1596=
XM_017011107.2:c.4767G>A	XP_016866596.1:p.Lys1589=
XR_002956289.1:n.5062G>A
NM_001363725.2:c.2616G>A	NP_001350654.1:p.Lys872=
NM_001371656.1:c.4995G>A	NP_001358585.1:p.Lys1665=
NM_001374820.1:c.4995G>A	NP_001361749.1:p.Lys1665=
NM_001374828.1:c.5115G>A MANE Select	NP_001361757.1:p.Lys1705=
NM_017519.3:c.4956G>A	NP_059989.3:p.Lys1652=