Canonical Allele Identifier: CA366241890

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522218A>C (hg19) ; chr6:g.157201084A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201084A>C , CM000668.2:g.157201084A>C	GRCh38
NC_000006.11:g.157522218A>C , CM000668.1:g.157522218A>C	GRCh37
NC_000006.10:g.157563910A>C	NCBI36
NG_032093.1:g.428155A>C
NG_032093.2:g.428155A>C
NG_066624.1:g.430059A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4700A>C	ENSP00000055163.8:p.Asp1567Ala
ENST00000414678.8:c.4769A>C	ENSP00000412835.3:p.Asp1590Ala
ENST00000637015.2:c.4988A>C	ENSP00000489729.2:p.Asp1663Ala
ENST00000346085.10:c.4739A>C	ENSP00000344546.5:p.Asp1580Ala
ENST00000350026.10:c.4451A>C	ENSP00000055163.7:p.Asp1484Ala
ENST00000414678.7:c.3017A>C	ENSP00000412835.2:p.Asp1006Ala
ENST00000635849.1:c.2180A>C	ENSP00000490948.1:p.Asp727Ala
ENST00000635957.1:c.1811A>C	ENSP00000490385.1:p.Asp604Ala
ENST00000636227.1:n.3322A>C
ENST00000636254.1:n.779A>C
ENST00000636930.2:c.4859A>C MANE Select	ENSP00000490491.2:p.Asp1620Ala
ENST00000636940.1:n.2856A>C
ENST00000637015.1:c.2227A>C
ENST00000637568.1:c.2141A>C
ENST00000637741.1:n.1525A>C
ENST00000637810.1:c.2201A>C	ENSP00000489636.1:p.Asp734Ala
ENST00000637904.1:c.2360A>C	ENSP00000490550.1:p.Asp787Ala
ENST00000647938.1:c.4490A>C	ENSP00000498155.1:p.Asp1497Ala
ENST00000346085.9:c.4490A>C	ENSP00000344546.4:p.Asp1497Ala
ENST00000350026.9:c.4451A>C	ENSP00000055163.7:p.Asp1484Ala
ENST00000414678.6:c.3017A>C	ENSP00000412835.2:p.Asp1006Ala
NM_017519.2:c.4451A>C	NP_059989.2:p.Asp1484Ala
NM_020732.3:c.4490A>C	NP_065783.3:p.Asp1497Ala
XM_005267069.3:c.4610A>C	XP_005267126.2:p.Asp1537Ala
XM_011535984.1:c.3689A>C	XP_011534286.1:p.Asp1230Ala
XM_011535985.1:c.3509A>C	XP_011534287.1:p.Asp1170Ala
XM_011535986.1:c.3269A>C	XP_011534288.1:p.Asp1090Ala
XM_011535987.1:c.2888A>C	XP_011534289.1:p.Asp963Ala
XM_011535988.1:c.1751A>C	XP_011534290.1:p.Asp584Ala
NM_001346813.1:c.4610A>C	NP_001333742.1:p.Asp1537Ala
NM_001363725.1:c.2360A>C	NP_001350654.1:p.Asp787Ala
XM_011535984.2:c.4820A>C	XP_011534286.2:p.Asp1607Ala
XM_011535988.3:c.1751A>C	XP_011534290.1:p.Asp584Ala
XM_017011103.2:c.4721A>C	XP_016866592.1:p.Asp1574Ala
XM_017011104.1:c.4691A>C	XP_016866593.1:p.Asp1564Ala
XM_017011105.2:c.4661A>C	XP_016866594.1:p.Asp1554Ala
XM_017011106.2:c.4532A>C	XP_016866595.1:p.Asp1511Ala
XM_017011107.2:c.4511A>C	XP_016866596.1:p.Asp1504Ala
XR_002956289.1:n.4806A>C
NM_001363725.2:c.2360A>C	NP_001350654.1:p.Asp787Ala
NM_001371656.1:c.4739A>C	NP_001358585.1:p.Asp1580Ala
NM_001374820.1:c.4739A>C	NP_001361749.1:p.Asp1580Ala
NM_001374828.1:c.4859A>C MANE Select	NP_001361757.1:p.Asp1620Ala
NM_017519.3:c.4700A>C	NP_059989.3:p.Asp1567Ala