Canonical Allele Identifier: CA366239937

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366752
• gnomAD v4: 6-157198909-T-G
• MyVariant Identifiers: chr6:g.157520043T>G (hg19) ; chr6:g.157198909T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198909T>G , CM000668.2:g.157198909T>G	GRCh38
NC_000006.11:g.157520043T>G , CM000668.1:g.157520043T>G	GRCh37
NC_000006.10:g.157561735T>G	NCBI36
NG_032093.1:g.425980T>G
NG_032093.2:g.425980T>G
NG_066624.1:g.427884T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4320+2T>G	ENSP00000055163.8:n.4320+2T>G
ENST00000414678.8:c.4389+2T>G	ENSP00000412835.3:n.4389+2T>G
ENST00000637015.2:c.4608+2T>G	ENSP00000489729.2:n.4608+2T>G
ENST00000346085.10:c.4359+2T>G	ENSP00000344546.5:n.4359+2T>G
ENST00000350026.10:c.4071+2T>G	ENSP00000055163.7:n.4071+2T>G
ENST00000414678.7:c.2637+2T>G	ENSP00000412835.2:n.2637+2T>G
ENST00000635849.1:c.1800+2T>G	ENSP00000490948.1:n.1800+2T>G
ENST00000635957.1:c.1431+2T>G	ENSP00000490385.1:n.1431+2T>G
ENST00000636227.1:n.2942+2T>G
ENST00000636254.1:n.399+2T>G
ENST00000636930.2:c.4479+2T>G MANE Select	ENSP00000490491.2:n.4479+2T>G
ENST00000636940.1:n.2476+2T>G
ENST00000637015.1:c.1847+2T>G
ENST00000637568.1:c.1761+2T>G
ENST00000637741.1:n.1145+2T>G
ENST00000637810.1:c.1821+2T>G	ENSP00000489636.1:n.1821+2T>G
ENST00000637904.1:c.1980+2T>G	ENSP00000490550.1:n.1980+2T>G
ENST00000647938.1:c.4110+2T>G	ENSP00000498155.1:n.4110+2T>G
ENST00000346085.9:c.4110+2T>G	ENSP00000344546.4:n.4110+2T>G
ENST00000350026.9:c.4071+2T>G	ENSP00000055163.7:n.4071+2T>G
ENST00000414678.6:c.2637+2T>G	ENSP00000412835.2:n.2637+2T>G
NM_017519.2:c.4071+2T>G	NP_059989.2:n.4071+2T>G
NM_020732.3:c.4110+2T>G	NP_065783.3:n.4110+2T>G
XM_005267069.3:c.4230+2T>G	XP_005267126.2:n.4230+2T>G
XM_011535984.1:c.3309+2T>G	XP_011534286.1:n.3309+2T>G
XM_011535985.1:c.3129+2T>G	XP_011534287.1:n.3129+2T>G
XM_011535986.1:c.2889+2T>G	XP_011534288.1:n.2889+2T>G
XM_011535987.1:c.2508+2T>G	XP_011534289.1:n.2508+2T>G
XM_011535988.1:c.1371+2T>G	XP_011534290.1:n.1371+2T>G
NM_001346813.1:c.4230+2T>G	NP_001333742.1:n.4230+2T>G
NM_001363725.1:c.1980+2T>G	NP_001350654.1:n.1980+2T>G
XM_011535984.2:c.4440+2T>G	XP_011534286.2:n.4440+2T>G
XM_011535988.3:c.1371+2T>G	XP_011534290.1:n.1371+2T>G
XM_017011103.2:c.4341+2T>G	XP_016866592.1:n.4341+2T>G
XM_017011104.1:c.4311+2T>G	XP_016866593.1:n.4311+2T>G
XM_017011105.2:c.4281+2T>G	XP_016866594.1:n.4281+2T>G
XM_017011106.2:c.4152+2T>G	XP_016866595.1:n.4152+2T>G
XM_017011107.2:c.4131+2T>G	XP_016866596.1:n.4131+2T>G
XR_002956289.1:n.4427-1796T>G
NM_001363725.2:c.1980+2T>G	NP_001350654.1:n.1980+2T>G
NM_001371656.1:c.4359+2T>G	NP_001358585.1:n.4359+2T>G
NM_001374820.1:c.4359+2T>G	NP_001361749.1:n.4359+2T>G
NM_001374828.1:c.4479+2T>G MANE Select	NP_001361757.1:n.4479+2T>G
NM_017519.3:c.4320+2T>G	NP_059989.3:n.4320+2T>G