Canonical Allele Identifier: CA452978032

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128325191
• MyVariant Identifiers: chr6:g.157505439C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157184305C>G , CM000668.2:g.157184305C>G	GRCh38
NC_000006.11:g.157505439C>G , CM000668.1:g.157505439C>G	GRCh37
NC_000006.10:g.157547131C>G	NCBI36
NG_032093.1:g.411376C>G
NG_032093.2:g.411376C>G
NG_066624.1:g.413280C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3630C>G	ENSP00000055163.8:p.Ser1210=
ENST00000414678.8:c.3699C>G	ENSP00000412835.3:p.Ser1233=
ENST00000637015.2:c.3918C>G	ENSP00000489729.2:p.Ser1306=
ENST00000319584.11:c.1803C>G	ENSP00000313006.7:p.Ser601=
ENST00000346085.10:c.3669C>G	ENSP00000344546.5:p.Ser1223=
ENST00000350026.10:c.3381C>G	ENSP00000055163.7:p.Ser1127=
ENST00000414678.7:c.1947C>G	ENSP00000412835.2:p.Ser649=
ENST00000635849.1:c.1110C>G	ENSP00000490948.1:p.Ser370=
ENST00000635957.1:c.744C>G	ENSP00000490385.1:p.Ser248=
ENST00000636930.2:c.3789C>G MANE Select	ENSP00000490491.2:p.Ser1263=
ENST00000636940.1:n.1786C>G
ENST00000637015.1:c.1157C>G
ENST00000637568.1:c.1071C>G
ENST00000637741.1:n.455C>G
ENST00000637810.1:c.1131C>G	ENSP00000489636.1:p.Ser377=
ENST00000637904.1:c.1290C>G	ENSP00000490550.1:p.Ser430=
ENST00000647938.1:c.3420C>G	ENSP00000498155.1:p.Ser1140=
ENST00000319584.10:c.1806C>G	ENSP00000313006.6:p.Ser602=
ENST00000346085.9:c.3420C>G	ENSP00000344546.4:p.Ser1140=
ENST00000350026.9:c.3381C>G	ENSP00000055163.7:p.Ser1127=
ENST00000400790.3:c.582C>G	ENSP00000383596.3:p.Ser194=
ENST00000414678.6:c.1947C>G	ENSP00000412835.2:p.Ser649=
NM_017519.2:c.3381C>G	NP_059989.2:p.Ser1127=
NM_020732.3:c.3420C>G	NP_065783.3:p.Ser1140=
XM_005267069.3:c.3540C>G	XP_005267126.2:p.Ser1180=
XM_011535984.1:c.2619C>G	XP_011534286.1:p.Ser873=
XM_011535985.1:c.2439C>G	XP_011534287.1:p.Ser813=
XM_011535986.1:c.2199C>G	XP_011534288.1:p.Ser733=
XM_011535987.1:c.1818C>G	XP_011534289.1:p.Ser606=
XM_011535988.1:c.681C>G	XP_011534290.1:p.Ser227=
NM_001346813.1:c.3540C>G	NP_001333742.1:p.Ser1180=
NM_001363725.1:c.1290C>G	NP_001350654.1:p.Ser430=
XM_011535984.2:c.3750C>G	XP_011534286.2:p.Ser1250=
XM_011535988.3:c.681C>G	XP_011534290.1:p.Ser227=
XM_017011103.2:c.3651C>G	XP_016866592.1:p.Ser1217=
XM_017011104.1:c.3621C>G	XP_016866593.1:p.Ser1207=
XM_017011105.2:c.3591C>G	XP_016866594.1:p.Ser1197=
XM_017011106.2:c.3462C>G	XP_016866595.1:p.Ser1154=
XM_017011107.2:c.3441C>G	XP_016866596.1:p.Ser1147=
XR_002956289.1:n.3833C>G
NM_001363725.2:c.1290C>G	NP_001350654.1:p.Ser430=
NM_001371656.1:c.3669C>G	NP_001358585.1:p.Ser1223=
NM_001374820.1:c.3669C>G	NP_001361749.1:p.Ser1223=
NM_001374828.1:c.3789C>G MANE Select	NP_001361757.1:p.Ser1263=
NM_017519.3:c.3630C>G	NP_059989.3:p.Ser1210=