Canonical Allele Identifier: CA366242053

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128374721
• MyVariant Identifiers: chr6:g.157522258C>A (hg19) ; chr6:g.157201124C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201124C>A , CM000668.2:g.157201124C>A	GRCh38
NC_000006.11:g.157522258C>A , CM000668.1:g.157522258C>A	GRCh37
NC_000006.10:g.157563950C>A	NCBI36
NG_032093.1:g.428195C>A
NG_032093.2:g.428195C>A
NG_066624.1:g.430099C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4740C>A	ENSP00000055163.8:p.Ser1580Arg
ENST00000414678.8:c.4809C>A	ENSP00000412835.3:p.Ser1603Arg
ENST00000637015.2:c.5028C>A	ENSP00000489729.2:p.Ser1676Arg
ENST00000346085.10:c.4779C>A	ENSP00000344546.5:p.Ser1593Arg
ENST00000350026.10:c.4491C>A	ENSP00000055163.7:p.Ser1497Arg
ENST00000414678.7:c.3057C>A	ENSP00000412835.2:p.Ser1019Arg
ENST00000635849.1:c.2220C>A	ENSP00000490948.1:p.Ser740Arg
ENST00000635957.1:c.1851C>A	ENSP00000490385.1:p.Ser617Arg
ENST00000636227.1:n.3362C>A
ENST00000636254.1:n.819C>A
ENST00000636930.2:c.4899C>A MANE Select	ENSP00000490491.2:p.Ser1633Arg
ENST00000636940.1:n.2896C>A
ENST00000637015.1:c.2267C>A
ENST00000637568.1:c.2181C>A
ENST00000637741.1:n.1565C>A
ENST00000637810.1:c.2241C>A	ENSP00000489636.1:p.Ser747Arg
ENST00000637904.1:c.2400C>A	ENSP00000490550.1:p.Ser800Arg
ENST00000647938.1:c.4530C>A	ENSP00000498155.1:p.Ser1510Arg
ENST00000346085.9:c.4530C>A	ENSP00000344546.4:p.Ser1510Arg
ENST00000350026.9:c.4491C>A	ENSP00000055163.7:p.Ser1497Arg
ENST00000414678.6:c.3057C>A	ENSP00000412835.2:p.Ser1019Arg
NM_017519.2:c.4491C>A	NP_059989.2:p.Ser1497Arg
NM_020732.3:c.4530C>A	NP_065783.3:p.Ser1510Arg
XM_005267069.3:c.4650C>A	XP_005267126.2:p.Ser1550Arg
XM_011535984.1:c.3729C>A	XP_011534286.1:p.Ser1243Arg
XM_011535985.1:c.3549C>A	XP_011534287.1:p.Ser1183Arg
XM_011535986.1:c.3309C>A	XP_011534288.1:p.Ser1103Arg
XM_011535987.1:c.2928C>A	XP_011534289.1:p.Ser976Arg
XM_011535988.1:c.1791C>A	XP_011534290.1:p.Ser597Arg
NM_001346813.1:c.4650C>A	NP_001333742.1:p.Ser1550Arg
NM_001363725.1:c.2400C>A	NP_001350654.1:p.Ser800Arg
XM_011535984.2:c.4860C>A	XP_011534286.2:p.Ser1620Arg
XM_011535988.3:c.1791C>A	XP_011534290.1:p.Ser597Arg
XM_017011103.2:c.4761C>A	XP_016866592.1:p.Ser1587Arg
XM_017011104.1:c.4731C>A	XP_016866593.1:p.Ser1577Arg
XM_017011105.2:c.4701C>A	XP_016866594.1:p.Ser1567Arg
XM_017011106.2:c.4572C>A	XP_016866595.1:p.Ser1524Arg
XM_017011107.2:c.4551C>A	XP_016866596.1:p.Ser1517Arg
XR_002956289.1:n.4846C>A
NM_001363725.2:c.2400C>A	NP_001350654.1:p.Ser800Arg
NM_001371656.1:c.4779C>A	NP_001358585.1:p.Ser1593Arg
NM_001374820.1:c.4779C>A	NP_001361749.1:p.Ser1593Arg
NM_001374828.1:c.4899C>A MANE Select	NP_001361757.1:p.Ser1633Arg
NM_017519.3:c.4740C>A	NP_059989.3:p.Ser1580Arg