Canonical Allele Identifier: CA366242260

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522349C>A (hg19) ; chr6:g.157201215C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201215C>A , CM000668.2:g.157201215C>A	GRCh38
NC_000006.11:g.157522349C>A , CM000668.1:g.157522349C>A	GRCh37
NC_000006.10:g.157564041C>A	NCBI36
NG_032093.1:g.428286C>A
NG_032093.2:g.428286C>A
NG_066624.1:g.430190C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4831C>A	ENSP00000055163.8:p.Gln1611Lys
ENST00000414678.8:c.4900C>A	ENSP00000412835.3:p.Gln1634Lys
ENST00000637015.2:c.5119C>A	ENSP00000489729.2:p.Gln1707Lys
ENST00000346085.10:c.4870C>A	ENSP00000344546.5:p.Gln1624Lys
ENST00000350026.10:c.4582C>A	ENSP00000055163.7:p.Gln1528Lys
ENST00000414678.7:c.3148C>A	ENSP00000412835.2:p.Gln1050Lys
ENST00000635849.1:c.2311C>A	ENSP00000490948.1:p.Gln771Lys
ENST00000635957.1:c.1942C>A	ENSP00000490385.1:p.Gln648Lys
ENST00000636227.1:n.3453C>A
ENST00000636254.1:n.910C>A
ENST00000636930.2:c.4990C>A MANE Select	ENSP00000490491.2:p.Gln1664Lys
ENST00000636940.1:n.2987C>A
ENST00000637015.1:c.2358C>A
ENST00000637568.1:c.2272C>A
ENST00000637741.1:n.1656C>A
ENST00000637810.1:c.2332C>A	ENSP00000489636.1:p.Gln778Lys
ENST00000637904.1:c.2491C>A	ENSP00000490550.1:p.Gln831Lys
ENST00000647938.1:c.4621C>A	ENSP00000498155.1:p.Gln1541Lys
ENST00000346085.9:c.4621C>A	ENSP00000344546.4:p.Gln1541Lys
ENST00000350026.9:c.4582C>A	ENSP00000055163.7:p.Gln1528Lys
ENST00000414678.6:c.3148C>A	ENSP00000412835.2:p.Gln1050Lys
NM_017519.2:c.4582C>A	NP_059989.2:p.Gln1528Lys
NM_020732.3:c.4621C>A	NP_065783.3:p.Gln1541Lys
XM_005267069.3:c.4741C>A	XP_005267126.2:p.Gln1581Lys
XM_011535984.1:c.3820C>A	XP_011534286.1:p.Gln1274Lys
XM_011535985.1:c.3640C>A	XP_011534287.1:p.Gln1214Lys
XM_011535986.1:c.3400C>A	XP_011534288.1:p.Gln1134Lys
XM_011535987.1:c.3019C>A	XP_011534289.1:p.Gln1007Lys
XM_011535988.1:c.1882C>A	XP_011534290.1:p.Gln628Lys
NM_001346813.1:c.4741C>A	NP_001333742.1:p.Gln1581Lys
NM_001363725.1:c.2491C>A	NP_001350654.1:p.Gln831Lys
XM_011535984.2:c.4951C>A	XP_011534286.2:p.Gln1651Lys
XM_011535988.3:c.1882C>A	XP_011534290.1:p.Gln628Lys
XM_017011103.2:c.4852C>A	XP_016866592.1:p.Gln1618Lys
XM_017011104.1:c.4822C>A	XP_016866593.1:p.Gln1608Lys
XM_017011105.2:c.4792C>A	XP_016866594.1:p.Gln1598Lys
XM_017011106.2:c.4663C>A	XP_016866595.1:p.Gln1555Lys
XM_017011107.2:c.4642C>A	XP_016866596.1:p.Gln1548Lys
XR_002956289.1:n.4937C>A
NM_001363725.2:c.2491C>A	NP_001350654.1:p.Gln831Lys
NM_001371656.1:c.4870C>A	NP_001358585.1:p.Gln1624Lys
NM_001374820.1:c.4870C>A	NP_001361749.1:p.Gln1624Lys
NM_001374828.1:c.4990C>A MANE Select	NP_001361757.1:p.Gln1664Lys
NM_017519.3:c.4831C>A	NP_059989.3:p.Gln1611Lys