Canonical Allele Identifier: CA366242350

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522393C>G (hg19) ; chr6:g.157201259C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201259C>G , CM000668.2:g.157201259C>G	GRCh38
NC_000006.11:g.157522393C>G , CM000668.1:g.157522393C>G	GRCh37
NC_000006.10:g.157564085C>G	NCBI36
NG_032093.1:g.428330C>G
NG_032093.2:g.428330C>G
NG_066624.1:g.430234C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4875C>G	ENSP00000055163.8:p.Ser1625Arg
ENST00000414678.8:c.4944C>G	ENSP00000412835.3:p.Ser1648Arg
ENST00000637015.2:c.5163C>G	ENSP00000489729.2:p.Ser1721Arg
ENST00000346085.10:c.4914C>G	ENSP00000344546.5:p.Ser1638Arg
ENST00000350026.10:c.4626C>G	ENSP00000055163.7:p.Ser1542Arg
ENST00000414678.7:c.3192C>G	ENSP00000412835.2:p.Ser1064Arg
ENST00000635849.1:c.2355C>G	ENSP00000490948.1:p.Ser785Arg
ENST00000635957.1:c.1986C>G	ENSP00000490385.1:p.Ser662Arg
ENST00000636227.1:n.3497C>G
ENST00000636254.1:n.954C>G
ENST00000636930.2:c.5034C>G MANE Select	ENSP00000490491.2:p.Ser1678Arg
ENST00000636940.1:n.3031C>G
ENST00000637015.1:c.2402C>G
ENST00000637568.1:c.2316C>G
ENST00000637741.1:n.1700C>G
ENST00000637810.1:c.2376C>G	ENSP00000489636.1:p.Ser792Arg
ENST00000637904.1:c.2535C>G	ENSP00000490550.1:p.Ser845Arg
ENST00000647938.1:c.4665C>G	ENSP00000498155.1:p.Ser1555Arg
ENST00000346085.9:c.4665C>G	ENSP00000344546.4:p.Ser1555Arg
ENST00000350026.9:c.4626C>G	ENSP00000055163.7:p.Ser1542Arg
ENST00000414678.6:c.3192C>G	ENSP00000412835.2:p.Ser1064Arg
NM_017519.2:c.4626C>G	NP_059989.2:p.Ser1542Arg
NM_020732.3:c.4665C>G	NP_065783.3:p.Ser1555Arg
XM_005267069.3:c.4785C>G	XP_005267126.2:p.Ser1595Arg
XM_011535984.1:c.3864C>G	XP_011534286.1:p.Ser1288Arg
XM_011535985.1:c.3684C>G	XP_011534287.1:p.Ser1228Arg
XM_011535986.1:c.3444C>G	XP_011534288.1:p.Ser1148Arg
XM_011535987.1:c.3063C>G	XP_011534289.1:p.Ser1021Arg
XM_011535988.1:c.1926C>G	XP_011534290.1:p.Ser642Arg
NM_001346813.1:c.4785C>G	NP_001333742.1:p.Ser1595Arg
NM_001363725.1:c.2535C>G	NP_001350654.1:p.Ser845Arg
XM_011535984.2:c.4995C>G	XP_011534286.2:p.Ser1665Arg
XM_011535988.3:c.1926C>G	XP_011534290.1:p.Ser642Arg
XM_017011103.2:c.4896C>G	XP_016866592.1:p.Ser1632Arg
XM_017011104.1:c.4866C>G	XP_016866593.1:p.Ser1622Arg
XM_017011105.2:c.4836C>G	XP_016866594.1:p.Ser1612Arg
XM_017011106.2:c.4707C>G	XP_016866595.1:p.Ser1569Arg
XM_017011107.2:c.4686C>G	XP_016866596.1:p.Ser1562Arg
XR_002956289.1:n.4981C>G
NM_001363725.2:c.2535C>G	NP_001350654.1:p.Ser845Arg
NM_001371656.1:c.4914C>G	NP_001358585.1:p.Ser1638Arg
NM_001374820.1:c.4914C>G	NP_001361749.1:p.Ser1638Arg
NM_001374828.1:c.5034C>G MANE Select	NP_001361757.1:p.Ser1678Arg
NM_017519.3:c.4875C>G	NP_059989.3:p.Ser1625Arg