Canonical Allele Identifier: CA150368741

Gene: ARID1B

Linked Data

• dbSNP Id: rs1019262791
• MyVariant Identifiers: chr6:g.157520211G>A (hg19) ; chr6:g.157199077G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157199077G>A , CM000668.2:g.157199077G>A	GRCh38
NC_000006.11:g.157520211G>A , CM000668.1:g.157520211G>A	GRCh37
NC_000006.10:g.157561903G>A	NCBI36
NG_032093.1:g.426148G>A
NG_032093.2:g.426148G>A
NG_066624.1:g.428052G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4320+170G>A	ENSP00000055163.8:n.4320+170G>A
ENST00000414678.8:c.4389+170G>A	ENSP00000412835.3:n.4389+170G>A
ENST00000637015.2:c.4608+170G>A	ENSP00000489729.2:n.4608+170G>A
ENST00000346085.10:c.4359+170G>A	ENSP00000344546.5:n.4359+170G>A
ENST00000350026.10:c.4071+170G>A	ENSP00000055163.7:n.4071+170G>A
ENST00000414678.7:c.2637+170G>A	ENSP00000412835.2:n.2637+170G>A
ENST00000635849.1:c.1800+170G>A	ENSP00000490948.1:n.1800+170G>A
ENST00000635957.1:c.1431+170G>A	ENSP00000490385.1:n.1431+170G>A
ENST00000636227.1:n.2942+170G>A
ENST00000636254.1:n.399+170G>A
ENST00000636930.2:c.4479+170G>A MANE Select	ENSP00000490491.2:n.4479+170G>A
ENST00000636940.1:n.2476+170G>A
ENST00000637015.1:c.1847+170G>A
ENST00000637568.1:c.1761+170G>A
ENST00000637741.1:n.1145+170G>A
ENST00000637810.1:c.1821+170G>A	ENSP00000489636.1:n.1821+170G>A
ENST00000637904.1:c.1980+170G>A	ENSP00000490550.1:n.1980+170G>A
ENST00000647938.1:c.4110+170G>A	ENSP00000498155.1:n.4110+170G>A
ENST00000346085.9:c.4110+170G>A	ENSP00000344546.4:n.4110+170G>A
ENST00000350026.9:c.4071+170G>A	ENSP00000055163.7:n.4071+170G>A
ENST00000414678.6:c.2637+170G>A	ENSP00000412835.2:n.2637+170G>A
NM_017519.2:c.4071+170G>A	NP_059989.2:n.4071+170G>A
NM_020732.3:c.4110+170G>A	NP_065783.3:n.4110+170G>A
XM_005267069.3:c.4230+170G>A	XP_005267126.2:n.4230+170G>A
XM_011535984.1:c.3309+170G>A	XP_011534286.1:n.3309+170G>A
XM_011535985.1:c.3129+170G>A	XP_011534287.1:n.3129+170G>A
XM_011535986.1:c.2889+170G>A	XP_011534288.1:n.2889+170G>A
XM_011535987.1:c.2508+170G>A	XP_011534289.1:n.2508+170G>A
XM_011535988.1:c.1371+170G>A	XP_011534290.1:n.1371+170G>A
NM_001346813.1:c.4230+170G>A	NP_001333742.1:n.4230+170G>A
NM_001363725.1:c.1980+170G>A	NP_001350654.1:n.1980+170G>A
XM_011535984.2:c.4440+170G>A	XP_011534286.2:n.4440+170G>A
XM_011535988.3:c.1371+170G>A	XP_011534290.1:n.1371+170G>A
XM_017011103.2:c.4341+170G>A	XP_016866592.1:n.4341+170G>A
XM_017011104.1:c.4311+170G>A	XP_016866593.1:n.4311+170G>A
XM_017011105.2:c.4281+170G>A	XP_016866594.1:n.4281+170G>A
XM_017011106.2:c.4152+170G>A	XP_016866595.1:n.4152+170G>A
XM_017011107.2:c.4131+170G>A	XP_016866596.1:n.4131+170G>A
XR_002956289.1:n.4427-1628G>A
NM_001363725.2:c.1980+170G>A	NP_001350654.1:n.1980+170G>A
NM_001371656.1:c.4359+170G>A	NP_001358585.1:n.4359+170G>A
NM_001374820.1:c.4359+170G>A	NP_001361749.1:n.4359+170G>A
NM_001374828.1:c.4479+170G>A MANE Select	NP_001361757.1:n.4479+170G>A
NM_017519.3:c.4320+170G>A	NP_059989.3:n.4320+170G>A