Canonical Allele Identifier: CA366388349

Gene: ARID1B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157133100C>G , CM000668.2:g.157133100C>G	GRCh38
NC_000006.11:g.157454234C>G , CM000668.1:g.157454234C>G	GRCh37
NC_000006.10:g.157495926C>G	NCBI36
NG_032093.1:g.360171C>G
NG_032093.2:g.360171C>G
NG_066624.1:g.362075C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2654C>G	ENSP00000055163.8:p.Ser885Trp
ENST00000414678.8:c.2564C>G	ENSP00000412835.3:p.Ser855Trp
ENST00000637015.2:c.2654C>G	ENSP00000489729.2:p.Ser885Trp
ENST00000319584.11:c.668C>G	ENSP00000313006.7:p.Ser223Trp
ENST00000346085.10:c.2693C>G	ENSP00000344546.5:p.Ser898Trp
ENST00000350026.10:c.2405C>G	ENSP00000055163.7:p.Ser802Trp
ENST00000414678.7:c.812C>G	ENSP00000412835.2:p.Ser271Trp
ENST00000452544.2:n.555C>G
ENST00000635849.1:c.83-15524C>G	ENSP00000490948.1:n.83-15524C>G
ENST00000636930.2:c.2654C>G MANE Select	ENSP00000490491.2:p.Ser885Trp
ENST00000637003.1:c.155C>G	ENSP00000489666.1:p.Ser52Trp
ENST00000637810.1:c.155C>G	ENSP00000489636.1:p.Ser52Trp
ENST00000637904.1:c.155C>G	ENSP00000490550.1:p.Ser52Trp
ENST00000647938.1:c.2444C>G	ENSP00000498155.1:p.Ser815Trp
ENST00000674190.1:n.1403C>G
ENST00000319584.10:c.671C>G	ENSP00000313006.6:p.Ser224Trp
ENST00000346085.9:c.2444C>G	ENSP00000344546.4:p.Ser815Trp
ENST00000350026.9:c.2405C>G	ENSP00000055163.7:p.Ser802Trp
ENST00000414678.6:c.812C>G	ENSP00000412835.2:p.Ser271Trp
ENST00000452544.1:n.501C>G
NM_017519.2:c.2405C>G	NP_059989.2:p.Ser802Trp
NM_020732.3:c.2444C>G	NP_065783.3:p.Ser815Trp
XM_005267069.3:c.2405C>G	XP_005267126.2:p.Ser802Trp
XM_011535984.1:c.1355C>G	XP_011534286.1:p.Ser452Trp
XM_011535985.1:c.1283-15524C>G	XP_011534287.1:n.1283-15524C>G
XM_011535986.1:c.935C>G	XP_011534288.1:p.Ser312Trp
XM_011535987.1:c.554C>G	XP_011534289.1:p.Ser185Trp
NM_001346813.1:c.2405C>G	NP_001333742.1:p.Ser802Trp
NM_001363725.1:c.155C>G	NP_001350654.1:p.Ser52Trp
XM_011535984.2:c.2486C>G	XP_011534286.2:p.Ser829Trp
XM_017011103.2:c.2486C>G	XP_016866592.1:p.Ser829Trp
XM_017011104.1:c.2486C>G	XP_016866593.1:p.Ser829Trp
XM_017011105.2:c.2486C>G	XP_016866594.1:p.Ser829Trp
XM_017011106.2:c.2486C>G	XP_016866595.1:p.Ser829Trp
XM_017011107.2:c.2414-15524C>G	XP_016866596.1:n.2414-15524C>G
XR_002956289.1:n.2569C>G
NM_001363725.2:c.155C>G	NP_001350654.1:p.Ser52Trp
NM_001371656.1:c.2693C>G	NP_001358585.1:p.Ser898Trp
NM_001374820.1:c.2693C>G	NP_001361749.1:p.Ser898Trp
NM_001374828.1:c.2654C>G MANE Select	NP_001361757.1:p.Ser885Trp
NM_017519.3:c.2654C>G	NP_059989.3:p.Ser885Trp