Canonical Allele Identifier: CA366242612

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522470A>C (hg19) ; chr6:g.157201336A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201336A>C , CM000668.2:g.157201336A>C	GRCh38
NC_000006.11:g.157522470A>C , CM000668.1:g.157522470A>C	GRCh37
NC_000006.10:g.157564162A>C	NCBI36
NG_032093.1:g.428407A>C
NG_032093.2:g.428407A>C
NG_066624.1:g.430311A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4952A>C	ENSP00000055163.8:p.Gln1651Pro
ENST00000414678.8:c.5021A>C	ENSP00000412835.3:p.Gln1674Pro
ENST00000637015.2:c.5240A>C	ENSP00000489729.2:p.Gln1747Pro
ENST00000346085.10:c.4991A>C	ENSP00000344546.5:p.Gln1664Pro
ENST00000350026.10:c.4703A>C	ENSP00000055163.7:p.Gln1568Pro
ENST00000414678.7:c.3269A>C	ENSP00000412835.2:p.Gln1090Pro
ENST00000635849.1:c.2432A>C	ENSP00000490948.1:p.Gln811Pro
ENST00000635957.1:c.2063A>C	ENSP00000490385.1:p.Gln688Pro
ENST00000636227.1:n.3574A>C
ENST00000636254.1:n.1031A>C
ENST00000636930.2:c.5111A>C MANE Select	ENSP00000490491.2:p.Gln1704Pro
ENST00000636940.1:n.3108A>C
ENST00000637015.1:c.2479A>C
ENST00000637568.1:c.2393A>C
ENST00000637741.1:n.1777A>C
ENST00000637810.1:c.2453A>C	ENSP00000489636.1:p.Gln818Pro
ENST00000637904.1:c.2612A>C	ENSP00000490550.1:p.Gln871Pro
ENST00000647938.1:c.4742A>C	ENSP00000498155.1:p.Gln1581Pro
ENST00000346085.9:c.4742A>C	ENSP00000344546.4:p.Gln1581Pro
ENST00000350026.9:c.4703A>C	ENSP00000055163.7:p.Gln1568Pro
ENST00000414678.6:c.3269A>C	ENSP00000412835.2:p.Gln1090Pro
NM_017519.2:c.4703A>C	NP_059989.2:p.Gln1568Pro
NM_020732.3:c.4742A>C	NP_065783.3:p.Gln1581Pro
XM_005267069.3:c.4862A>C	XP_005267126.2:p.Gln1621Pro
XM_011535984.1:c.3941A>C	XP_011534286.1:p.Gln1314Pro
XM_011535985.1:c.3761A>C	XP_011534287.1:p.Gln1254Pro
XM_011535986.1:c.3521A>C	XP_011534288.1:p.Gln1174Pro
XM_011535987.1:c.3140A>C	XP_011534289.1:p.Gln1047Pro
XM_011535988.1:c.2003A>C	XP_011534290.1:p.Gln668Pro
NM_001346813.1:c.4862A>C	NP_001333742.1:p.Gln1621Pro
NM_001363725.1:c.2612A>C	NP_001350654.1:p.Gln871Pro
XM_011535984.2:c.5072A>C	XP_011534286.2:p.Gln1691Pro
XM_011535988.3:c.2003A>C	XP_011534290.1:p.Gln668Pro
XM_017011103.2:c.4973A>C	XP_016866592.1:p.Gln1658Pro
XM_017011104.1:c.4943A>C	XP_016866593.1:p.Gln1648Pro
XM_017011105.2:c.4913A>C	XP_016866594.1:p.Gln1638Pro
XM_017011106.2:c.4784A>C	XP_016866595.1:p.Gln1595Pro
XM_017011107.2:c.4763A>C	XP_016866596.1:p.Gln1588Pro
XR_002956289.1:n.5058A>C
NM_001363725.2:c.2612A>C	NP_001350654.1:p.Gln871Pro
NM_001371656.1:c.4991A>C	NP_001358585.1:p.Gln1664Pro
NM_001374820.1:c.4991A>C	NP_001361749.1:p.Gln1664Pro
NM_001374828.1:c.5111A>C MANE Select	NP_001361757.1:p.Gln1704Pro
NM_017519.3:c.4952A>C	NP_059989.3:p.Gln1651Pro