Canonical Allele Identifier: CA452978226

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201247-C-T
• MyVariant Identifiers: chr6:g.157522381C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201247C>T , CM000668.2:g.157201247C>T	GRCh38
NC_000006.11:g.157522381C>T , CM000668.1:g.157522381C>T	GRCh37
NC_000006.10:g.157564073C>T	NCBI36
NG_032093.1:g.428318C>T
NG_032093.2:g.428318C>T
NG_066624.1:g.430222C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4863C>T	ENSP00000055163.8:p.Ser1621=
ENST00000414678.8:c.4932C>T	ENSP00000412835.3:p.Ser1644=
ENST00000637015.2:c.5151C>T	ENSP00000489729.2:p.Ser1717=
ENST00000346085.10:c.4902C>T	ENSP00000344546.5:p.Ser1634=
ENST00000350026.10:c.4614C>T	ENSP00000055163.7:p.Ser1538=
ENST00000414678.7:c.3180C>T	ENSP00000412835.2:p.Ser1060=
ENST00000635849.1:c.2343C>T	ENSP00000490948.1:p.Ser781=
ENST00000635957.1:c.1974C>T	ENSP00000490385.1:p.Ser658=
ENST00000636227.1:n.3485C>T
ENST00000636254.1:n.942C>T
ENST00000636930.2:c.5022C>T MANE Select	ENSP00000490491.2:p.Ser1674=
ENST00000636940.1:n.3019C>T
ENST00000637015.1:c.2390C>T
ENST00000637568.1:c.2304C>T
ENST00000637741.1:n.1688C>T
ENST00000637810.1:c.2364C>T	ENSP00000489636.1:p.Ser788=
ENST00000637904.1:c.2523C>T	ENSP00000490550.1:p.Ser841=
ENST00000647938.1:c.4653C>T	ENSP00000498155.1:p.Ser1551=
ENST00000346085.9:c.4653C>T	ENSP00000344546.4:p.Ser1551=
ENST00000350026.9:c.4614C>T	ENSP00000055163.7:p.Ser1538=
ENST00000414678.6:c.3180C>T	ENSP00000412835.2:p.Ser1060=
NM_017519.2:c.4614C>T	NP_059989.2:p.Ser1538=
NM_020732.3:c.4653C>T	NP_065783.3:p.Ser1551=
XM_005267069.3:c.4773C>T	XP_005267126.2:p.Ser1591=
XM_011535984.1:c.3852C>T	XP_011534286.1:p.Ser1284=
XM_011535985.1:c.3672C>T	XP_011534287.1:p.Ser1224=
XM_011535986.1:c.3432C>T	XP_011534288.1:p.Ser1144=
XM_011535987.1:c.3051C>T	XP_011534289.1:p.Ser1017=
XM_011535988.1:c.1914C>T	XP_011534290.1:p.Ser638=
NM_001346813.1:c.4773C>T	NP_001333742.1:p.Ser1591=
NM_001363725.1:c.2523C>T	NP_001350654.1:p.Ser841=
XM_011535984.2:c.4983C>T	XP_011534286.2:p.Ser1661=
XM_011535988.3:c.1914C>T	XP_011534290.1:p.Ser638=
XM_017011103.2:c.4884C>T	XP_016866592.1:p.Ser1628=
XM_017011104.1:c.4854C>T	XP_016866593.1:p.Ser1618=
XM_017011105.2:c.4824C>T	XP_016866594.1:p.Ser1608=
XM_017011106.2:c.4695C>T	XP_016866595.1:p.Ser1565=
XM_017011107.2:c.4674C>T	XP_016866596.1:p.Ser1558=
XR_002956289.1:n.4969C>T
NM_001363725.2:c.2523C>T	NP_001350654.1:p.Ser841=
NM_001371656.1:c.4902C>T	NP_001358585.1:p.Ser1634=
NM_001374820.1:c.4902C>T	NP_001361749.1:p.Ser1634=
NM_001374828.1:c.5022C>T MANE Select	NP_001361757.1:p.Ser1674=
NM_017519.3:c.4863C>T	NP_059989.3:p.Ser1621=