Canonical Allele Identifier: CA366387503

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128463514
• MyVariant Identifiers: chr6:g.157406041T>G (hg19) ; chr6:g.157084907T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157084907T>G , CM000668.2:g.157084907T>G	GRCh38
NC_000006.11:g.157406041T>G , CM000668.1:g.157406041T>G	GRCh37
NC_000006.10:g.157447733T>G	NCBI36
NG_032093.1:g.311978T>G
NG_032093.2:g.311978T>G
NG_066624.1:g.313882T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2491+2T>G	ENSP00000055163.8:n.2491+2T>G
ENST00000414678.8:c.2491+2T>G	ENSP00000412835.3:n.2491+2T>G
ENST00000637015.2:c.2491+2T>G	ENSP00000489729.2:n.2491+2T>G
ENST00000319584.11:c.505+2T>G	ENSP00000313006.7:n.505+2T>G
ENST00000346085.10:c.2530+2T>G	ENSP00000344546.5:n.2530+2T>G
ENST00000350026.10:c.2242+2T>G	ENSP00000055163.7:n.2242+2T>G
ENST00000414678.7:c.739+2T>G	ENSP00000412835.2:n.739+2T>G
ENST00000452544.2:n.392+2T>G
ENST00000493658.2:n.140+2T>G
ENST00000635849.1:c.-9+2T>G	ENSP00000490948.1:n.-9+2T>G
ENST00000636930.2:c.2491+2T>G MANE Select	ENSP00000490491.2:n.2491+2T>G
ENST00000637003.1:c.-9+2T>G	ENSP00000489666.1:n.-9+2T>G
ENST00000637810.1:c.-9+2T>G	ENSP00000489636.1:n.-9+2T>G
ENST00000637904.1:c.-9+2T>G	ENSP00000490550.1:n.-9+2T>G
ENST00000647938.1:c.2281+2T>G	ENSP00000498155.1:n.2281+2T>G
ENST00000674190.1:n.1240+2T>G
ENST00000319584.10:c.508+2T>G	ENSP00000313006.6:n.508+2T>G
ENST00000346085.9:c.2281+2T>G	ENSP00000344546.4:n.2281+2T>G
ENST00000350026.9:c.2242+2T>G	ENSP00000055163.7:n.2242+2T>G
ENST00000414678.6:c.739+2T>G	ENSP00000412835.2:n.739+2T>G
ENST00000452544.1:n.350+2T>G
ENST00000493658.1:n.140+2T>G
NM_017519.2:c.2242+2T>G	NP_059989.2:n.2242+2T>G
NM_020732.3:c.2281+2T>G	NP_065783.3:n.2281+2T>G
XM_005267069.3:c.2242+2T>G	XP_005267126.2:n.2242+2T>G
XM_011535984.1:c.1192+2T>G	XP_011534286.1:n.1192+2T>G
XM_011535985.1:c.1192+2T>G	XP_011534287.1:n.1192+2T>G
XM_011535986.1:c.772+2T>G	XP_011534288.1:n.772+2T>G
XM_011535987.1:c.391+2T>G	XP_011534289.1:n.391+2T>G
NM_001346813.1:c.2242+2T>G	NP_001333742.1:n.2242+2T>G
NM_001363725.1:c.-9+2T>G	NP_001350654.1:n.-9+2T>G
XM_011535984.2:c.2323+2T>G	XP_011534286.2:n.2323+2T>G
XM_017011103.2:c.2323+2T>G	XP_016866592.1:n.2323+2T>G
XM_017011104.1:c.2323+2T>G	XP_016866593.1:n.2323+2T>G
XM_017011105.2:c.2323+2T>G	XP_016866594.1:n.2323+2T>G
XM_017011106.2:c.2323+2T>G	XP_016866595.1:n.2323+2T>G
XM_017011107.2:c.2323+2T>G	XP_016866596.1:n.2323+2T>G
XR_002956289.1:n.2406+2T>G
NM_001363725.2:c.-9+2T>G	NP_001350654.1:n.-9+2T>G
NM_001371656.1:c.2530+2T>G	NP_001358585.1:n.2530+2T>G
NM_001374820.1:c.2530+2T>G	NP_001361749.1:n.2530+2T>G
NM_001374828.1:c.2491+2T>G MANE Select	NP_001361757.1:n.2491+2T>G
NM_017519.3:c.2491+2T>G	NP_059989.3:n.2491+2T>G