Canonical Allele Identifier: CA366243331

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1344548
• ClinVar RCV Id: RCV001848638 ; RCV002246549
• dbSNP Id: rs2128377544
• MyVariant Identifiers: chr6:g.157522623G>T (hg19) ; chr6:g.157201489G>T (hg38)
• MutSpliceDB: CA366243331

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201489G>T , CM000668.2:g.157201489G>T	GRCh38
NC_000006.11:g.157522623G>T , CM000668.1:g.157522623G>T	GRCh37
NC_000006.10:g.157564315G>T	NCBI36
NG_032093.1:g.428560G>T
NG_032093.2:g.428560G>T
NG_066624.1:g.430464G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.5104+1G>T	ENSP00000055163.8:n.5104+1G>T
ENST00000414678.8:c.5173+1G>T	ENSP00000412835.3:n.5173+1G>T
ENST00000637015.2:c.5392+1G>T	ENSP00000489729.2:n.5392+1G>T
ENST00000346085.10:c.5143+1G>T	ENSP00000344546.5:n.5143+1G>T
ENST00000350026.10:c.4855+1G>T	ENSP00000055163.7:n.4855+1G>T
ENST00000414678.7:c.3421+1G>T	ENSP00000412835.2:n.3421+1G>T
ENST00000635849.1:c.2584+1G>T	ENSP00000490948.1:n.2584+1G>T
ENST00000635957.1:c.2215+1G>T	ENSP00000490385.1:n.2215+1G>T
ENST00000636227.1:n.3726+1G>T
ENST00000636254.1:n.1183+1G>T
ENST00000636930.2:c.5263+1G>T MANE Select	ENSP00000490491.2:n.5263+1G>T
ENST00000636940.1:n.3260+1G>T
ENST00000637015.1:c.2631+1G>T
ENST00000637568.1:c.2545+1G>T
ENST00000637741.1:n.1929+1G>T
ENST00000637810.1:c.2605+1G>T	ENSP00000489636.1:n.2605+1G>T
ENST00000637904.1:c.2764+1G>T	ENSP00000490550.1:n.2764+1G>T
ENST00000647938.1:c.4894+1G>T	ENSP00000498155.1:n.4894+1G>T
ENST00000346085.9:c.4894+1G>T	ENSP00000344546.4:n.4894+1G>T
ENST00000350026.9:c.4855+1G>T	ENSP00000055163.7:n.4855+1G>T
ENST00000414678.6:c.3421+1G>T	ENSP00000412835.2:n.3421+1G>T
NM_017519.2:c.4855+1G>T	NP_059989.2:n.4855+1G>T
NM_020732.3:c.4894+1G>T	NP_065783.3:n.4894+1G>T
XM_005267069.3:c.5014+1G>T	XP_005267126.2:n.5014+1G>T
XM_011535984.1:c.4093+1G>T	XP_011534286.1:n.4093+1G>T
XM_011535985.1:c.3913+1G>T	XP_011534287.1:n.3913+1G>T
XM_011535986.1:c.3673+1G>T	XP_011534288.1:n.3673+1G>T
XM_011535987.1:c.3292+1G>T	XP_011534289.1:n.3292+1G>T
XM_011535988.1:c.2155+1G>T	XP_011534290.1:n.2155+1G>T
NM_001346813.1:c.5014+1G>T	NP_001333742.1:n.5014+1G>T
NM_001363725.1:c.2764+1G>T	NP_001350654.1:n.2764+1G>T
XM_011535984.2:c.5224+1G>T	XP_011534286.2:n.5224+1G>T
XM_011535988.3:c.2155+1G>T	XP_011534290.1:n.2155+1G>T
XM_017011103.2:c.5125+1G>T	XP_016866592.1:n.5125+1G>T
XM_017011104.1:c.5095+1G>T	XP_016866593.1:n.5095+1G>T
XM_017011105.2:c.5065+1G>T	XP_016866594.1:n.5065+1G>T
XM_017011106.2:c.4936+1G>T	XP_016866595.1:n.4936+1G>T
XM_017011107.2:c.4915+1G>T	XP_016866596.1:n.4915+1G>T
XR_002956289.1:n.5210+1G>T
NM_001363725.2:c.2764+1G>T	NP_001350654.1:n.2764+1G>T
NM_001371656.1:c.5143+1G>T	NP_001358585.1:n.5143+1G>T
NM_001374820.1:c.5143+1G>T	NP_001361749.1:n.5143+1G>T
NM_001374828.1:c.5263+1G>T MANE Select	NP_001361757.1:n.5263+1G>T
NM_017519.3:c.5104+1G>T	NP_059989.3:n.5104+1G>T