Canonical Allele Identifier: CA452978216

Gene: ARID1B

Linked Data

• dbSNP Id: rs1468561084
• gnomAD v2: 6-157522375-C-T
• gnomAD v4: 6-157201241-C-T
• MyVariant Identifiers: chr6:g.157522375C>T (hg19) ; chr6:g.157201241C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201241C>T , CM000668.2:g.157201241C>T	GRCh38
NC_000006.11:g.157522375C>T , CM000668.1:g.157522375C>T	GRCh37
NC_000006.10:g.157564067C>T	NCBI36
NG_032093.1:g.428312C>T
NG_032093.2:g.428312C>T
NG_066624.1:g.430216C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4857C>T	ENSP00000055163.8:p.His1619=
ENST00000414678.8:c.4926C>T	ENSP00000412835.3:p.His1642=
ENST00000637015.2:c.5145C>T	ENSP00000489729.2:p.His1715=
ENST00000346085.10:c.4896C>T	ENSP00000344546.5:p.His1632=
ENST00000350026.10:c.4608C>T	ENSP00000055163.7:p.His1536=
ENST00000414678.7:c.3174C>T	ENSP00000412835.2:p.His1058=
ENST00000635849.1:c.2337C>T	ENSP00000490948.1:p.His779=
ENST00000635957.1:c.1968C>T	ENSP00000490385.1:p.His656=
ENST00000636227.1:n.3479C>T
ENST00000636254.1:n.936C>T
ENST00000636930.2:c.5016C>T MANE Select	ENSP00000490491.2:p.His1672=
ENST00000636940.1:n.3013C>T
ENST00000637015.1:c.2384C>T
ENST00000637568.1:c.2298C>T
ENST00000637741.1:n.1682C>T
ENST00000637810.1:c.2358C>T	ENSP00000489636.1:p.His786=
ENST00000637904.1:c.2517C>T	ENSP00000490550.1:p.His839=
ENST00000647938.1:c.4647C>T	ENSP00000498155.1:p.His1549=
ENST00000346085.9:c.4647C>T	ENSP00000344546.4:p.His1549=
ENST00000350026.9:c.4608C>T	ENSP00000055163.7:p.His1536=
ENST00000414678.6:c.3174C>T	ENSP00000412835.2:p.His1058=
NM_017519.2:c.4608C>T	NP_059989.2:p.His1536=
NM_020732.3:c.4647C>T	NP_065783.3:p.His1549=
XM_005267069.3:c.4767C>T	XP_005267126.2:p.His1589=
XM_011535984.1:c.3846C>T	XP_011534286.1:p.His1282=
XM_011535985.1:c.3666C>T	XP_011534287.1:p.His1222=
XM_011535986.1:c.3426C>T	XP_011534288.1:p.His1142=
XM_011535987.1:c.3045C>T	XP_011534289.1:p.His1015=
XM_011535988.1:c.1908C>T	XP_011534290.1:p.His636=
NM_001346813.1:c.4767C>T	NP_001333742.1:p.His1589=
NM_001363725.1:c.2517C>T	NP_001350654.1:p.His839=
XM_011535984.2:c.4977C>T	XP_011534286.2:p.His1659=
XM_011535988.3:c.1908C>T	XP_011534290.1:p.His636=
XM_017011103.2:c.4878C>T	XP_016866592.1:p.His1626=
XM_017011104.1:c.4848C>T	XP_016866593.1:p.His1616=
XM_017011105.2:c.4818C>T	XP_016866594.1:p.His1606=
XM_017011106.2:c.4689C>T	XP_016866595.1:p.His1563=
XM_017011107.2:c.4668C>T	XP_016866596.1:p.His1556=
XR_002956289.1:n.4963C>T
NM_001363725.2:c.2517C>T	NP_001350654.1:p.His839=
NM_001371656.1:c.4896C>T	NP_001358585.1:p.His1632=
NM_001374820.1:c.4896C>T	NP_001361749.1:p.His1632=
NM_001374828.1:c.5016C>T MANE Select	NP_001361757.1:p.His1672=
NM_017519.3:c.4857C>T	NP_059989.3:p.His1619=