Canonical Allele Identifier: CA366228512

Gene: ARID1B

Linked Data

• dbSNP Id: rs864309615
• MyVariant Identifiers: chr6:g.157502302G>C (hg19) ; chr6:g.157181168G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181168G>C , CM000668.2:g.157181168G>C	GRCh38
NC_000006.11:g.157502302G>C , CM000668.1:g.157502302G>C	GRCh37
NC_000006.10:g.157543994G>C	NCBI36
NG_032093.1:g.408239G>C
NG_032093.2:g.408239G>C
NG_066624.1:g.410143G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3545G>C	ENSP00000055163.8:p.Gly1182Ala
ENST00000414678.8:c.3614G>C	ENSP00000412835.3:p.Gly1205Ala
ENST00000637015.2:c.3833G>C	ENSP00000489729.2:p.Gly1278Ala
ENST00000319584.11:c.1718G>C	ENSP00000313006.7:p.Gly573Ala
ENST00000346085.10:c.3584G>C	ENSP00000344546.5:p.Gly1195Ala
ENST00000350026.10:c.3296G>C	ENSP00000055163.7:p.Gly1099Ala
ENST00000414678.7:c.1862G>C	ENSP00000412835.2:p.Gly621Ala
ENST00000635849.1:c.1025G>C	ENSP00000490948.1:p.Gly342Ala
ENST00000635957.1:c.659G>C	ENSP00000490385.1:p.Gly220Ala
ENST00000636930.2:c.3704G>C MANE Select	ENSP00000490491.2:p.Gly1235Ala
ENST00000636940.1:n.1701G>C
ENST00000637015.1:c.1072G>C
ENST00000637568.1:c.986G>C
ENST00000637741.1:n.370G>C
ENST00000637810.1:c.1046G>C	ENSP00000489636.1:p.Gly349Ala
ENST00000637904.1:c.1205G>C	ENSP00000490550.1:p.Gly402Ala
ENST00000647938.1:c.3335G>C	ENSP00000498155.1:p.Gly1112Ala
ENST00000319584.10:c.1721G>C	ENSP00000313006.6:p.Gly574Ala
ENST00000346085.9:c.3335G>C	ENSP00000344546.4:p.Gly1112Ala
ENST00000350026.9:c.3296G>C	ENSP00000055163.7:p.Gly1099Ala
ENST00000400790.3:c.497G>C	ENSP00000383596.3:p.Gly166Ala
ENST00000414678.6:c.1862G>C	ENSP00000412835.2:p.Gly621Ala
ENST00000478761.3:c.906G>C
NM_017519.2:c.3296G>C	NP_059989.2:p.Gly1099Ala
NM_020732.3:c.3335G>C	NP_065783.3:p.Gly1112Ala
XM_005267069.3:c.3455G>C	XP_005267126.2:p.Gly1152Ala
XM_011535984.1:c.2534G>C	XP_011534286.1:p.Gly845Ala
XM_011535985.1:c.2354G>C	XP_011534287.1:p.Gly785Ala
XM_011535986.1:c.2114G>C	XP_011534288.1:p.Gly705Ala
XM_011535987.1:c.1733G>C	XP_011534289.1:p.Gly578Ala
XM_011535988.1:c.596G>C	XP_011534290.1:p.Gly199Ala
NM_001346813.1:c.3455G>C	NP_001333742.1:p.Gly1152Ala
NM_001363725.1:c.1205G>C	NP_001350654.1:p.Gly402Ala
XM_011535984.2:c.3665G>C	XP_011534286.2:p.Gly1222Ala
XM_011535988.3:c.596G>C	XP_011534290.1:p.Gly199Ala
XM_017011103.2:c.3566G>C	XP_016866592.1:p.Gly1189Ala
XM_017011104.1:c.3536G>C	XP_016866593.1:p.Gly1179Ala
XM_017011105.2:c.3506G>C	XP_016866594.1:p.Gly1169Ala
XM_017011106.2:c.3377G>C	XP_016866595.1:p.Gly1126Ala
XM_017011107.2:c.3356G>C	XP_016866596.1:p.Gly1119Ala
XR_002956289.1:n.3748G>C
NM_001363725.2:c.1205G>C	NP_001350654.1:p.Gly402Ala
NM_001371656.1:c.3584G>C	NP_001358585.1:p.Gly1195Ala
NM_001374820.1:c.3584G>C	NP_001361749.1:p.Gly1195Ala
NM_001374828.1:c.3704G>C MANE Select	NP_001361757.1:p.Gly1235Ala
NM_017519.3:c.3545G>C	NP_059989.3:p.Gly1182Ala