Canonical Allele Identifier: CA16042552
Gene: ARID1B HGNC NCBI

Linked Data

ClinVar Variation Id: 373155
ClinVar RCV Id: RCV000412794
dbSNP Id: rs1057518256

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.156778698G>T , CM000668.2:g.156778698G>T GRCh38
NC_000006.11:g.157099832G>T , CM000668.1:g.157099832G>T GRCh37
NC_000006.10:g.157141524G>T NCBI36
NG_032093.1:g.5769G>T
NG_032093.2:g.5769G>T
NG_066624.1:g.7673G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000350026.11:c.1018G>T ENSP00000055163.8:p.Gly340Ter
ENST00000414678.8:c.1018G>T ENSP00000412835.3:p.Gly340Ter
ENST00000637015.2:c.1018G>T ENSP00000489729.2:p.Gly340Ter
ENST00000346085.10:c.1018G>T ENSP00000344546.5:p.Gly340Ter
ENST00000350026.10:c.769G>T ENSP00000055163.7:p.Gly257Ter
ENST00000636930.2:c.1018G>T MANE Select ENSP00000490491.2:p.Gly340Ter
ENST00000647938.1:c.769G>T ENSP00000498155.1:p.Gly257Ter
ENST00000674298.1:c.758G>T
ENST00000346085.9:c.769G>T ENSP00000344546.4:p.Gly257Ter
ENST00000350026.9:c.769G>T ENSP00000055163.7:p.Gly257Ter
NM_017519.2:c.769G>T NP_059989.2:p.Gly257Ter
NM_020732.3:c.769G>T NP_065783.3:p.Gly257Ter
XM_005267069.3:c.769G>T XP_005267126.2:p.Gly257Ter
NM_001346813.1:c.769G>T NP_001333742.1:p.Gly257Ter
XM_011535984.2:c.769G>T XP_011534286.2:p.Gly257Ter
XM_017011103.2:c.769G>T XP_016866592.1:p.Gly257Ter
XM_017011104.1:c.769G>T XP_016866593.1:p.Gly257Ter
XM_017011105.2:c.769G>T XP_016866594.1:p.Gly257Ter
XM_017011106.2:c.769G>T XP_016866595.1:p.Gly257Ter
XM_017011107.2:c.769G>T XP_016866596.1:p.Gly257Ter
XR_002956289.1:n.852G>T
NM_001371656.1:c.1018G>T NP_001358585.1:p.Gly340Ter
NM_001374820.1:c.1018G>T NP_001361749.1:p.Gly340Ter
NM_001374828.1:c.1018G>T MANE Select NP_001361757.1:p.Gly340Ter
NM_017519.3:c.1018G>T NP_059989.3:p.Gly340Ter