Canonical Allele Identifier: CA452989824

Gene: ARID1B

Linked Data

• dbSNP Id: rs962858324
• MyVariant Identifiers: chr6:g.157406017A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084883A>C , CM000668.2:g.157084883A>C	GRCh38
NC_000006.11:g.157406017A>C , CM000668.1:g.157406017A>C	GRCh37
NC_000006.10:g.157447709A>C	NCBI36
NG_032093.1:g.311954A>C
NG_032093.2:g.311954A>C
NG_066624.1:g.313858A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2469A>C	ENSP00000055163.8:p.Pro823=
ENST00000414678.8:c.2469A>C	ENSP00000412835.3:p.Pro823=
ENST00000637015.2:c.2469A>C	ENSP00000489729.2:p.Pro823=
ENST00000319584.11:c.483A>C	ENSP00000313006.7:p.Pro161=
ENST00000346085.10:c.2508A>C	ENSP00000344546.5:p.Pro836=
ENST00000350026.10:c.2220A>C	ENSP00000055163.7:p.Pro740=
ENST00000414678.7:c.717A>C	ENSP00000412835.2:p.Pro239=
ENST00000452544.2:n.370A>C
ENST00000493658.2:n.118A>C
ENST00000635849.1:c.-31A>C	ENSP00000490948.1:n.-31A>C
ENST00000636930.2:c.2469A>C MANE Select	ENSP00000490491.2:p.Pro823=
ENST00000637003.1:c.-31A>C	ENSP00000489666.1:n.-31A>C
ENST00000637810.1:c.-31A>C	ENSP00000489636.1:n.-31A>C
ENST00000637904.1:c.-31A>C	ENSP00000490550.1:n.-31A>C
ENST00000647938.1:c.2259A>C	ENSP00000498155.1:p.Pro753=
ENST00000674190.1:n.1218A>C
ENST00000319584.10:c.486A>C	ENSP00000313006.6:p.Pro162=
ENST00000346085.9:c.2259A>C	ENSP00000344546.4:p.Pro753=
ENST00000350026.9:c.2220A>C	ENSP00000055163.7:p.Pro740=
ENST00000414678.6:c.717A>C	ENSP00000412835.2:p.Pro239=
ENST00000452544.1:n.328A>C
ENST00000493658.1:n.118A>C
NM_017519.2:c.2220A>C	NP_059989.2:p.Pro740=
NM_020732.3:c.2259A>C	NP_065783.3:p.Pro753=
XM_005267069.3:c.2220A>C	XP_005267126.2:p.Pro740=
XM_011535984.1:c.1170A>C	XP_011534286.1:p.Pro390=
XM_011535985.1:c.1170A>C	XP_011534287.1:p.Pro390=
XM_011535986.1:c.750A>C	XP_011534288.1:p.Pro250=
XM_011535987.1:c.369A>C	XP_011534289.1:p.Pro123=
NM_001346813.1:c.2220A>C	NP_001333742.1:p.Pro740=
NM_001363725.1:c.-31A>C	NP_001350654.1:n.-31A>C
XM_011535984.2:c.2301A>C	XP_011534286.2:p.Pro767=
XM_017011103.2:c.2301A>C	XP_016866592.1:p.Pro767=
XM_017011104.1:c.2301A>C	XP_016866593.1:p.Pro767=
XM_017011105.2:c.2301A>C	XP_016866594.1:p.Pro767=
XM_017011106.2:c.2301A>C	XP_016866595.1:p.Pro767=
XM_017011107.2:c.2301A>C	XP_016866596.1:p.Pro767=
XR_002956289.1:n.2384A>C
NM_001363725.2:c.-31A>C	NP_001350654.1:n.-31A>C
NM_001371656.1:c.2508A>C	NP_001358585.1:p.Pro836=
NM_001374820.1:c.2508A>C	NP_001361749.1:p.Pro836=
NM_001374828.1:c.2469A>C MANE Select	NP_001361757.1:p.Pro823=
NM_017519.3:c.2469A>C	NP_059989.3:p.Pro823=