Canonical Allele Identifier: CA366234956

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511207A>C (hg19) ; chr6:g.157190073A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190073A>C , CM000668.2:g.157190073A>C	GRCh38
NC_000006.11:g.157511207A>C , CM000668.1:g.157511207A>C	GRCh37
NC_000006.10:g.157552899A>C	NCBI36
NG_032093.1:g.417144A>C
NG_032093.2:g.417144A>C
NG_066624.1:g.419048A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3935A>C	ENSP00000055163.8:p.Asp1312Ala
ENST00000414678.8:c.4004A>C	ENSP00000412835.3:p.Asp1335Ala
ENST00000637015.2:c.4223A>C	ENSP00000489729.2:p.Asp1408Ala
ENST00000346085.10:c.3974A>C	ENSP00000344546.5:p.Asp1325Ala
ENST00000350026.10:c.3686A>C	ENSP00000055163.7:p.Asp1229Ala
ENST00000414678.7:c.2252A>C	ENSP00000412835.2:p.Asp751Ala
ENST00000635849.1:c.1415A>C	ENSP00000490948.1:p.Asp472Ala
ENST00000635957.1:c.1046A>C	ENSP00000490385.1:p.Asp349Ala
ENST00000636930.2:c.4094A>C MANE Select	ENSP00000490491.2:p.Asp1365Ala
ENST00000636940.1:n.2091A>C
ENST00000637015.1:c.1462A>C
ENST00000637568.1:c.1376A>C
ENST00000637741.1:n.760A>C
ENST00000637810.1:c.1436A>C	ENSP00000489636.1:p.Asp479Ala
ENST00000637904.1:c.1595A>C	ENSP00000490550.1:p.Asp532Ala
ENST00000647938.1:c.3725A>C	ENSP00000498155.1:p.Asp1242Ala
ENST00000346085.9:c.3725A>C	ENSP00000344546.4:p.Asp1242Ala
ENST00000350026.9:c.3686A>C	ENSP00000055163.7:p.Asp1229Ala
ENST00000414678.6:c.2252A>C	ENSP00000412835.2:p.Asp751Ala
NM_017519.2:c.3686A>C	NP_059989.2:p.Asp1229Ala
NM_020732.3:c.3725A>C	NP_065783.3:p.Asp1242Ala
XM_005267069.3:c.3845A>C	XP_005267126.2:p.Asp1282Ala
XM_011535984.1:c.2924A>C	XP_011534286.1:p.Asp975Ala
XM_011535985.1:c.2744A>C	XP_011534287.1:p.Asp915Ala
XM_011535986.1:c.2504A>C	XP_011534288.1:p.Asp835Ala
XM_011535987.1:c.2123A>C	XP_011534289.1:p.Asp708Ala
XM_011535988.1:c.986A>C	XP_011534290.1:p.Asp329Ala
NM_001346813.1:c.3845A>C	NP_001333742.1:p.Asp1282Ala
NM_001363725.1:c.1595A>C	NP_001350654.1:p.Asp532Ala
XM_011535984.2:c.4055A>C	XP_011534286.2:p.Asp1352Ala
XM_011535988.3:c.986A>C	XP_011534290.1:p.Asp329Ala
XM_017011103.2:c.3956A>C	XP_016866592.1:p.Asp1319Ala
XM_017011104.1:c.3926A>C	XP_016866593.1:p.Asp1309Ala
XM_017011105.2:c.3896A>C	XP_016866594.1:p.Asp1299Ala
XM_017011106.2:c.3767A>C	XP_016866595.1:p.Asp1256Ala
XM_017011107.2:c.3746A>C	XP_016866596.1:p.Asp1249Ala
XR_002956289.1:n.4138A>C
NM_001363725.2:c.1595A>C	NP_001350654.1:p.Asp532Ala
NM_001371656.1:c.3974A>C	NP_001358585.1:p.Asp1325Ala
NM_001374820.1:c.3974A>C	NP_001361749.1:p.Asp1325Ala
NM_001374828.1:c.4094A>C MANE Select	NP_001361757.1:p.Asp1365Ala
NM_017519.3:c.3935A>C	NP_059989.3:p.Asp1312Ala