Canonical Allele Identifier: CA366387303

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128462888
• MyVariant Identifiers: chr6:g.157405938A>C (hg19) ; chr6:g.157084804A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084804A>C , CM000668.2:g.157084804A>C	GRCh38
NC_000006.11:g.157405938A>C , CM000668.1:g.157405938A>C	GRCh37
NC_000006.10:g.157447630A>C	NCBI36
NG_032093.1:g.311875A>C
NG_032093.2:g.311875A>C
NG_066624.1:g.313779A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2390A>C	ENSP00000055163.8:p.His797Pro
ENST00000414678.8:c.2390A>C	ENSP00000412835.3:p.His797Pro
ENST00000637015.2:c.2390A>C	ENSP00000489729.2:p.His797Pro
ENST00000319584.11:c.404A>C	ENSP00000313006.7:p.His135Pro
ENST00000346085.10:c.2429A>C	ENSP00000344546.5:p.His810Pro
ENST00000350026.10:c.2141A>C	ENSP00000055163.7:p.His714Pro
ENST00000414678.7:c.638A>C	ENSP00000412835.2:p.His213Pro
ENST00000452544.2:n.291A>C
ENST00000493658.2:n.39A>C
ENST00000635849.1:c.-110A>C	ENSP00000490948.1:n.-110A>C
ENST00000636930.2:c.2390A>C MANE Select	ENSP00000490491.2:p.His797Pro
ENST00000637003.1:c.-110A>C	ENSP00000489666.1:n.-110A>C
ENST00000637810.1:c.-110A>C	ENSP00000489636.1:n.-110A>C
ENST00000637904.1:c.-110A>C	ENSP00000490550.1:n.-110A>C
ENST00000647938.1:c.2180A>C	ENSP00000498155.1:p.His727Pro
ENST00000674190.1:n.1139A>C
ENST00000319584.10:c.407A>C	ENSP00000313006.6:p.His136Pro
ENST00000346085.9:c.2180A>C	ENSP00000344546.4:p.His727Pro
ENST00000350026.9:c.2141A>C	ENSP00000055163.7:p.His714Pro
ENST00000414678.6:c.638A>C	ENSP00000412835.2:p.His213Pro
ENST00000452544.1:n.249A>C
ENST00000493658.1:n.39A>C
NM_017519.2:c.2141A>C	NP_059989.2:p.His714Pro
NM_020732.3:c.2180A>C	NP_065783.3:p.His727Pro
XM_005267069.3:c.2141A>C	XP_005267126.2:p.His714Pro
XM_011535984.1:c.1091A>C	XP_011534286.1:p.His364Pro
XM_011535985.1:c.1091A>C	XP_011534287.1:p.His364Pro
XM_011535986.1:c.671A>C	XP_011534288.1:p.His224Pro
XM_011535987.1:c.290A>C	XP_011534289.1:p.His97Pro
NM_001346813.1:c.2141A>C	NP_001333742.1:p.His714Pro
NM_001363725.1:c.-110A>C	NP_001350654.1:n.-110A>C
XM_011535984.2:c.2222A>C	XP_011534286.2:p.His741Pro
XM_017011103.2:c.2222A>C	XP_016866592.1:p.His741Pro
XM_017011104.1:c.2222A>C	XP_016866593.1:p.His741Pro
XM_017011105.2:c.2222A>C	XP_016866594.1:p.His741Pro
XM_017011106.2:c.2222A>C	XP_016866595.1:p.His741Pro
XM_017011107.2:c.2222A>C	XP_016866596.1:p.His741Pro
XR_002956289.1:n.2305A>C
NM_001363725.2:c.-110A>C	NP_001350654.1:n.-110A>C
NM_001371656.1:c.2429A>C	NP_001358585.1:p.His810Pro
NM_001374820.1:c.2429A>C	NP_001361749.1:p.His810Pro
NM_001374828.1:c.2390A>C MANE Select	NP_001361757.1:p.His797Pro
NM_017519.3:c.2390A>C	NP_059989.3:p.His797Pro