Canonical Allele Identifier: CA452989820

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157406011T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084877T>G , CM000668.2:g.157084877T>G	GRCh38
NC_000006.11:g.157406011T>G , CM000668.1:g.157406011T>G	GRCh37
NC_000006.10:g.157447703T>G	NCBI36
NG_032093.1:g.311948T>G
NG_032093.2:g.311948T>G
NG_066624.1:g.313852T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2463T>G	ENSP00000055163.8:p.Ser821=
ENST00000414678.8:c.2463T>G	ENSP00000412835.3:p.Ser821=
ENST00000637015.2:c.2463T>G	ENSP00000489729.2:p.Ser821=
ENST00000319584.11:c.477T>G	ENSP00000313006.7:p.Ser159=
ENST00000346085.10:c.2502T>G	ENSP00000344546.5:p.Ser834=
ENST00000350026.10:c.2214T>G	ENSP00000055163.7:p.Ser738=
ENST00000414678.7:c.711T>G	ENSP00000412835.2:p.Ser237=
ENST00000452544.2:n.364T>G
ENST00000493658.2:n.112T>G
ENST00000635849.1:c.-37T>G	ENSP00000490948.1:n.-37T>G
ENST00000636930.2:c.2463T>G MANE Select	ENSP00000490491.2:p.Ser821=
ENST00000637003.1:c.-37T>G	ENSP00000489666.1:n.-37T>G
ENST00000637810.1:c.-37T>G	ENSP00000489636.1:n.-37T>G
ENST00000637904.1:c.-37T>G	ENSP00000490550.1:n.-37T>G
ENST00000647938.1:c.2253T>G	ENSP00000498155.1:p.Ser751=
ENST00000674190.1:n.1212T>G
ENST00000319584.10:c.480T>G	ENSP00000313006.6:p.Ser160=
ENST00000346085.9:c.2253T>G	ENSP00000344546.4:p.Ser751=
ENST00000350026.9:c.2214T>G	ENSP00000055163.7:p.Ser738=
ENST00000414678.6:c.711T>G	ENSP00000412835.2:p.Ser237=
ENST00000452544.1:n.322T>G
ENST00000493658.1:n.112T>G
NM_017519.2:c.2214T>G	NP_059989.2:p.Ser738=
NM_020732.3:c.2253T>G	NP_065783.3:p.Ser751=
XM_005267069.3:c.2214T>G	XP_005267126.2:p.Ser738=
XM_011535984.1:c.1164T>G	XP_011534286.1:p.Ser388=
XM_011535985.1:c.1164T>G	XP_011534287.1:p.Ser388=
XM_011535986.1:c.744T>G	XP_011534288.1:p.Ser248=
XM_011535987.1:c.363T>G	XP_011534289.1:p.Ser121=
NM_001346813.1:c.2214T>G	NP_001333742.1:p.Ser738=
NM_001363725.1:c.-37T>G	NP_001350654.1:n.-37T>G
XM_011535984.2:c.2295T>G	XP_011534286.2:p.Ser765=
XM_017011103.2:c.2295T>G	XP_016866592.1:p.Ser765=
XM_017011104.1:c.2295T>G	XP_016866593.1:p.Ser765=
XM_017011105.2:c.2295T>G	XP_016866594.1:p.Ser765=
XM_017011106.2:c.2295T>G	XP_016866595.1:p.Ser765=
XM_017011107.2:c.2295T>G	XP_016866596.1:p.Ser765=
XR_002956289.1:n.2378T>G
NM_001363725.2:c.-37T>G	NP_001350654.1:n.-37T>G
NM_001371656.1:c.2502T>G	NP_001358585.1:p.Ser834=
NM_001374820.1:c.2502T>G	NP_001361749.1:p.Ser834=
NM_001374828.1:c.2463T>G MANE Select	NP_001361757.1:p.Ser821=
NM_017519.3:c.2463T>G	NP_059989.3:p.Ser821=