Canonical Allele Identifier: CA366380895
Gene: ARID1B HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.156777946G>C , CM000668.2:g.156777946G>C GRCh38
NC_000006.11:g.157099080G>C , CM000668.1:g.157099080G>C GRCh37
NC_000006.10:g.157140772G>C NCBI36
NG_032093.1:g.5017G>C
NG_032093.2:g.5017G>C
NG_066624.1:g.6921G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000350026.11:c.266G>C ENSP00000055163.8:p.Gly89Ala
ENST00000414678.8:c.266G>C ENSP00000412835.3:p.Gly89Ala
ENST00000637015.2:c.266G>C ENSP00000489729.2:p.Gly89Ala
ENST00000346085.10:c.266G>C ENSP00000344546.5:p.Gly89Ala
ENST00000350026.10:c.17G>C ENSP00000055163.7:p.Gly6Ala
ENST00000636930.2:c.266G>C MANE Select ENSP00000490491.2:p.Gly89Ala
ENST00000647938.1:c.17G>C ENSP00000498155.1:p.Gly6Ala
ENST00000674298.1:c.6G>C
ENST00000346085.9:c.17G>C ENSP00000344546.4:p.Gly6Ala
ENST00000350026.9:c.17G>C ENSP00000055163.7:p.Gly6Ala
NM_017519.2:c.17G>C NP_059989.2:p.Gly6Ala
NM_020732.3:c.17G>C NP_065783.3:p.Gly6Ala
XM_005267069.3:c.17G>C XP_005267126.2:p.Gly6Ala
XR_943148.1:n.177+300C>G
NM_001346813.1:c.17G>C NP_001333742.1:p.Gly6Ala
XM_011535984.2:c.17G>C XP_011534286.2:p.Gly6Ala
XM_017011103.2:c.17G>C XP_016866592.1:p.Gly6Ala
XM_017011104.1:c.17G>C XP_016866593.1:p.Gly6Ala
XM_017011105.2:c.17G>C XP_016866594.1:p.Gly6Ala
XM_017011106.2:c.17G>C XP_016866595.1:p.Gly6Ala
XM_017011107.2:c.17G>C XP_016866596.1:p.Gly6Ala
XR_002956289.1:n.100G>C
NM_001371656.1:c.266G>C NP_001358585.1:p.Gly89Ala
NM_001374820.1:c.266G>C NP_001361749.1:p.Gly89Ala
NM_001374828.1:c.266G>C MANE Select NP_001361757.1:p.Gly89Ala
NM_017519.3:c.266G>C NP_059989.3:p.Gly89Ala
NR_163974.1:n.273+300C>G