Canonical Allele Identifier: CA366239633

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366109
• MyVariant Identifiers: chr6:g.157519974G>C (hg19) ; chr6:g.157198840G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198840G>C , CM000668.2:g.157198840G>C	GRCh38
NC_000006.11:g.157519974G>C , CM000668.1:g.157519974G>C	GRCh37
NC_000006.10:g.157561666G>C	NCBI36
NG_032093.1:g.425911G>C
NG_032093.2:g.425911G>C
NG_066624.1:g.427815G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4253G>C	ENSP00000055163.8:p.Gly1418Ala
ENST00000414678.8:c.4322G>C	ENSP00000412835.3:p.Gly1441Ala
ENST00000637015.2:c.4541G>C	ENSP00000489729.2:p.Gly1514Ala
ENST00000346085.10:c.4292G>C	ENSP00000344546.5:p.Gly1431Ala
ENST00000350026.10:c.4004G>C	ENSP00000055163.7:p.Gly1335Ala
ENST00000414678.7:c.2570G>C	ENSP00000412835.2:p.Gly857Ala
ENST00000635849.1:c.1733G>C	ENSP00000490948.1:p.Gly578Ala
ENST00000635957.1:c.1364G>C	ENSP00000490385.1:p.Gly455Ala
ENST00000636227.1:n.2875G>C
ENST00000636254.1:n.332G>C
ENST00000636930.2:c.4412G>C MANE Select	ENSP00000490491.2:p.Gly1471Ala
ENST00000636940.1:n.2409G>C
ENST00000637015.1:c.1780G>C
ENST00000637568.1:c.1694G>C
ENST00000637741.1:n.1078G>C
ENST00000637810.1:c.1754G>C	ENSP00000489636.1:p.Gly585Ala
ENST00000637904.1:c.1913G>C	ENSP00000490550.1:p.Gly638Ala
ENST00000647938.1:c.4043G>C	ENSP00000498155.1:p.Gly1348Ala
ENST00000346085.9:c.4043G>C	ENSP00000344546.4:p.Gly1348Ala
ENST00000350026.9:c.4004G>C	ENSP00000055163.7:p.Gly1335Ala
ENST00000414678.6:c.2570G>C	ENSP00000412835.2:p.Gly857Ala
NM_017519.2:c.4004G>C	NP_059989.2:p.Gly1335Ala
NM_020732.3:c.4043G>C	NP_065783.3:p.Gly1348Ala
XM_005267069.3:c.4163G>C	XP_005267126.2:p.Gly1388Ala
XM_011535984.1:c.3242G>C	XP_011534286.1:p.Gly1081Ala
XM_011535985.1:c.3062G>C	XP_011534287.1:p.Gly1021Ala
XM_011535986.1:c.2822G>C	XP_011534288.1:p.Gly941Ala
XM_011535987.1:c.2441G>C	XP_011534289.1:p.Gly814Ala
XM_011535988.1:c.1304G>C	XP_011534290.1:p.Gly435Ala
NM_001346813.1:c.4163G>C	NP_001333742.1:p.Gly1388Ala
NM_001363725.1:c.1913G>C	NP_001350654.1:p.Gly638Ala
XM_011535984.2:c.4373G>C	XP_011534286.2:p.Gly1458Ala
XM_011535988.3:c.1304G>C	XP_011534290.1:p.Gly435Ala
XM_017011103.2:c.4274G>C	XP_016866592.1:p.Gly1425Ala
XM_017011104.1:c.4244G>C	XP_016866593.1:p.Gly1415Ala
XM_017011105.2:c.4214G>C	XP_016866594.1:p.Gly1405Ala
XM_017011106.2:c.4085G>C	XP_016866595.1:p.Gly1362Ala
XM_017011107.2:c.4064G>C	XP_016866596.1:p.Gly1355Ala
XR_002956289.1:n.4427-1865G>C
NM_001363725.2:c.1913G>C	NP_001350654.1:p.Gly638Ala
NM_001371656.1:c.4292G>C	NP_001358585.1:p.Gly1431Ala
NM_001374820.1:c.4292G>C	NP_001361749.1:p.Gly1431Ala
NM_001374828.1:c.4412G>C MANE Select	NP_001361757.1:p.Gly1471Ala
NM_017519.3:c.4253G>C	NP_059989.3:p.Gly1418Ala