Canonical Allele Identifier: CA366234294

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128339044
• MyVariant Identifiers: chr6:g.157510898C>A (hg19) ; chr6:g.157189764C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189764C>A , CM000668.2:g.157189764C>A	GRCh38
NC_000006.11:g.157510898C>A , CM000668.1:g.157510898C>A	GRCh37
NC_000006.10:g.157552590C>A	NCBI36
NG_032093.1:g.416835C>A
NG_032093.2:g.416835C>A
NG_066624.1:g.418739C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3883C>A	ENSP00000055163.8:p.Pro1295Thr
ENST00000414678.8:c.3952C>A	ENSP00000412835.3:p.Pro1318Thr
ENST00000637015.2:c.4171C>A	ENSP00000489729.2:p.Pro1391Thr
ENST00000346085.10:c.3922C>A	ENSP00000344546.5:p.Pro1308Thr
ENST00000350026.10:c.3634C>A	ENSP00000055163.7:p.Pro1212Thr
ENST00000414678.7:c.2200C>A	ENSP00000412835.2:p.Pro734Thr
ENST00000635849.1:c.1363C>A	ENSP00000490948.1:p.Pro455Thr
ENST00000635957.1:c.997C>A	ENSP00000490385.1:p.Pro333Thr
ENST00000636930.2:c.4042C>A MANE Select	ENSP00000490491.2:p.Pro1348Thr
ENST00000636940.1:n.2039C>A
ENST00000637015.1:c.1410C>A
ENST00000637568.1:c.1324C>A
ENST00000637741.1:n.708C>A
ENST00000637810.1:c.1384C>A	ENSP00000489636.1:p.Pro462Thr
ENST00000637904.1:c.1543C>A	ENSP00000490550.1:p.Pro515Thr
ENST00000647938.1:c.3673C>A	ENSP00000498155.1:p.Pro1225Thr
ENST00000346085.9:c.3673C>A	ENSP00000344546.4:p.Pro1225Thr
ENST00000350026.9:c.3634C>A	ENSP00000055163.7:p.Pro1212Thr
ENST00000414678.6:c.2200C>A	ENSP00000412835.2:p.Pro734Thr
NM_017519.2:c.3634C>A	NP_059989.2:p.Pro1212Thr
NM_020732.3:c.3673C>A	NP_065783.3:p.Pro1225Thr
XM_005267069.3:c.3793C>A	XP_005267126.2:p.Pro1265Thr
XM_011535984.1:c.2872C>A	XP_011534286.1:p.Pro958Thr
XM_011535985.1:c.2692C>A	XP_011534287.1:p.Pro898Thr
XM_011535986.1:c.2452C>A	XP_011534288.1:p.Pro818Thr
XM_011535987.1:c.2071C>A	XP_011534289.1:p.Pro691Thr
XM_011535988.1:c.934C>A	XP_011534290.1:p.Pro312Thr
NM_001346813.1:c.3793C>A	NP_001333742.1:p.Pro1265Thr
NM_001363725.1:c.1543C>A	NP_001350654.1:p.Pro515Thr
XM_011535984.2:c.4003C>A	XP_011534286.2:p.Pro1335Thr
XM_011535988.3:c.934C>A	XP_011534290.1:p.Pro312Thr
XM_017011103.2:c.3904C>A	XP_016866592.1:p.Pro1302Thr
XM_017011104.1:c.3874C>A	XP_016866593.1:p.Pro1292Thr
XM_017011105.2:c.3844C>A	XP_016866594.1:p.Pro1282Thr
XM_017011106.2:c.3715C>A	XP_016866595.1:p.Pro1239Thr
XM_017011107.2:c.3694C>A	XP_016866596.1:p.Pro1232Thr
XR_002956289.1:n.4086C>A
NM_001363725.2:c.1543C>A	NP_001350654.1:p.Pro515Thr
NM_001371656.1:c.3922C>A	NP_001358585.1:p.Pro1308Thr
NM_001374820.1:c.3922C>A	NP_001361749.1:p.Pro1308Thr
NM_001374828.1:c.4042C>A MANE Select	NP_001361757.1:p.Pro1348Thr
NM_017519.3:c.3883C>A	NP_059989.3:p.Pro1295Thr