Canonical Allele Identifier: CA366242333

Gene: ARID1B

Linked Data

• dbSNP Id: rs1794096456
• gnomAD v4: 6-157201251-G-A
• MyVariant Identifiers: chr6:g.157522385G>A (hg19) ; chr6:g.157201251G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201251G>A , CM000668.2:g.157201251G>A	GRCh38
NC_000006.11:g.157522385G>A , CM000668.1:g.157522385G>A	GRCh37
NC_000006.10:g.157564077G>A	NCBI36
NG_032093.1:g.428322G>A
NG_032093.2:g.428322G>A
NG_066624.1:g.430226G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4867G>A	ENSP00000055163.8:p.Ala1623Thr
ENST00000414678.8:c.4936G>A	ENSP00000412835.3:p.Ala1646Thr
ENST00000637015.2:c.5155G>A	ENSP00000489729.2:p.Ala1719Thr
ENST00000346085.10:c.4906G>A	ENSP00000344546.5:p.Ala1636Thr
ENST00000350026.10:c.4618G>A	ENSP00000055163.7:p.Ala1540Thr
ENST00000414678.7:c.3184G>A	ENSP00000412835.2:p.Ala1062Thr
ENST00000635849.1:c.2347G>A	ENSP00000490948.1:p.Ala783Thr
ENST00000635957.1:c.1978G>A	ENSP00000490385.1:p.Ala660Thr
ENST00000636227.1:n.3489G>A
ENST00000636254.1:n.946G>A
ENST00000636930.2:c.5026G>A MANE Select	ENSP00000490491.2:p.Ala1676Thr
ENST00000636940.1:n.3023G>A
ENST00000637015.1:c.2394G>A
ENST00000637568.1:c.2308G>A
ENST00000637741.1:n.1692G>A
ENST00000637810.1:c.2368G>A	ENSP00000489636.1:p.Ala790Thr
ENST00000637904.1:c.2527G>A	ENSP00000490550.1:p.Ala843Thr
ENST00000647938.1:c.4657G>A	ENSP00000498155.1:p.Ala1553Thr
ENST00000346085.9:c.4657G>A	ENSP00000344546.4:p.Ala1553Thr
ENST00000350026.9:c.4618G>A	ENSP00000055163.7:p.Ala1540Thr
ENST00000414678.6:c.3184G>A	ENSP00000412835.2:p.Ala1062Thr
NM_017519.2:c.4618G>A	NP_059989.2:p.Ala1540Thr
NM_020732.3:c.4657G>A	NP_065783.3:p.Ala1553Thr
XM_005267069.3:c.4777G>A	XP_005267126.2:p.Ala1593Thr
XM_011535984.1:c.3856G>A	XP_011534286.1:p.Ala1286Thr
XM_011535985.1:c.3676G>A	XP_011534287.1:p.Ala1226Thr
XM_011535986.1:c.3436G>A	XP_011534288.1:p.Ala1146Thr
XM_011535987.1:c.3055G>A	XP_011534289.1:p.Ala1019Thr
XM_011535988.1:c.1918G>A	XP_011534290.1:p.Ala640Thr
NM_001346813.1:c.4777G>A	NP_001333742.1:p.Ala1593Thr
NM_001363725.1:c.2527G>A	NP_001350654.1:p.Ala843Thr
XM_011535984.2:c.4987G>A	XP_011534286.2:p.Ala1663Thr
XM_011535988.3:c.1918G>A	XP_011534290.1:p.Ala640Thr
XM_017011103.2:c.4888G>A	XP_016866592.1:p.Ala1630Thr
XM_017011104.1:c.4858G>A	XP_016866593.1:p.Ala1620Thr
XM_017011105.2:c.4828G>A	XP_016866594.1:p.Ala1610Thr
XM_017011106.2:c.4699G>A	XP_016866595.1:p.Ala1567Thr
XM_017011107.2:c.4678G>A	XP_016866596.1:p.Ala1560Thr
XR_002956289.1:n.4973G>A
NM_001363725.2:c.2527G>A	NP_001350654.1:p.Ala843Thr
NM_001371656.1:c.4906G>A	NP_001358585.1:p.Ala1636Thr
NM_001374820.1:c.4906G>A	NP_001361749.1:p.Ala1636Thr
NM_001374828.1:c.5026G>A MANE Select	NP_001361757.1:p.Ala1676Thr
NM_017519.3:c.4867G>A	NP_059989.3:p.Ala1623Thr