Canonical Allele Identifier: CA366387388

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128463156
• MyVariant Identifiers: chr6:g.157405983C>A (hg19) ; chr6:g.157084849C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084849C>A , CM000668.2:g.157084849C>A	GRCh38
NC_000006.11:g.157405983C>A , CM000668.1:g.157405983C>A	GRCh37
NC_000006.10:g.157447675C>A	NCBI36
NG_032093.1:g.311920C>A
NG_032093.2:g.311920C>A
NG_066624.1:g.313824C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2435C>A	ENSP00000055163.8:p.Ser812Tyr
ENST00000414678.8:c.2435C>A	ENSP00000412835.3:p.Ser812Tyr
ENST00000637015.2:c.2435C>A	ENSP00000489729.2:p.Ser812Tyr
ENST00000319584.11:c.449C>A	ENSP00000313006.7:p.Ser150Tyr
ENST00000346085.10:c.2474C>A	ENSP00000344546.5:p.Ser825Tyr
ENST00000350026.10:c.2186C>A	ENSP00000055163.7:p.Ser729Tyr
ENST00000414678.7:c.683C>A	ENSP00000412835.2:p.Ser228Tyr
ENST00000452544.2:n.336C>A
ENST00000493658.2:n.84C>A
ENST00000635849.1:c.-65C>A	ENSP00000490948.1:n.-65C>A
ENST00000636930.2:c.2435C>A MANE Select	ENSP00000490491.2:p.Ser812Tyr
ENST00000637003.1:c.-65C>A	ENSP00000489666.1:n.-65C>A
ENST00000637810.1:c.-65C>A	ENSP00000489636.1:n.-65C>A
ENST00000637904.1:c.-65C>A	ENSP00000490550.1:n.-65C>A
ENST00000647938.1:c.2225C>A	ENSP00000498155.1:p.Ser742Tyr
ENST00000674190.1:n.1184C>A
ENST00000319584.10:c.452C>A	ENSP00000313006.6:p.Ser151Tyr
ENST00000346085.9:c.2225C>A	ENSP00000344546.4:p.Ser742Tyr
ENST00000350026.9:c.2186C>A	ENSP00000055163.7:p.Ser729Tyr
ENST00000414678.6:c.683C>A	ENSP00000412835.2:p.Ser228Tyr
ENST00000452544.1:n.294C>A
ENST00000493658.1:n.84C>A
NM_017519.2:c.2186C>A	NP_059989.2:p.Ser729Tyr
NM_020732.3:c.2225C>A	NP_065783.3:p.Ser742Tyr
XM_005267069.3:c.2186C>A	XP_005267126.2:p.Ser729Tyr
XM_011535984.1:c.1136C>A	XP_011534286.1:p.Ser379Tyr
XM_011535985.1:c.1136C>A	XP_011534287.1:p.Ser379Tyr
XM_011535986.1:c.716C>A	XP_011534288.1:p.Ser239Tyr
XM_011535987.1:c.335C>A	XP_011534289.1:p.Ser112Tyr
NM_001346813.1:c.2186C>A	NP_001333742.1:p.Ser729Tyr
NM_001363725.1:c.-65C>A	NP_001350654.1:n.-65C>A
XM_011535984.2:c.2267C>A	XP_011534286.2:p.Ser756Tyr
XM_017011103.2:c.2267C>A	XP_016866592.1:p.Ser756Tyr
XM_017011104.1:c.2267C>A	XP_016866593.1:p.Ser756Tyr
XM_017011105.2:c.2267C>A	XP_016866594.1:p.Ser756Tyr
XM_017011106.2:c.2267C>A	XP_016866595.1:p.Ser756Tyr
XM_017011107.2:c.2267C>A	XP_016866596.1:p.Ser756Tyr
XR_002956289.1:n.2350C>A
NM_001363725.2:c.-65C>A	NP_001350654.1:n.-65C>A
NM_001371656.1:c.2474C>A	NP_001358585.1:p.Ser825Tyr
NM_001374820.1:c.2474C>A	NP_001361749.1:p.Ser825Tyr
NM_001374828.1:c.2435C>A MANE Select	NP_001361757.1:p.Ser812Tyr
NM_017519.3:c.2435C>A	NP_059989.3:p.Ser812Tyr