Canonical Allele Identifier: CA129764

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 31210
• ClinVar RCV Id: RCV000024209 ; RCV000254764 ; RCV001533118
• dbSNP Id: rs387907141
• MyVariant Identifiers: chr6:g.157502271C>T (hg19) ; chr6:g.157181137C>T (hg38)
• PubMed: PMID:22405089 ; PMID:22426308

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181137C>T , CM000668.2:g.157181137C>T	GRCh38
NC_000006.11:g.157502271C>T , CM000668.1:g.157502271C>T	GRCh37
NC_000006.10:g.157543963C>T	NCBI36
NG_032093.1:g.408208C>T
NG_032093.2:g.408208C>T
NG_066624.1:g.410112C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3514C>T	ENSP00000055163.8:p.Arg1172Ter
ENST00000414678.8:c.3583C>T	ENSP00000412835.3:p.Arg1195Ter
ENST00000637015.2:c.3802C>T	ENSP00000489729.2:p.Arg1268Ter
ENST00000319584.11:c.1687C>T	ENSP00000313006.7:p.Arg563Ter
ENST00000346085.10:c.3553C>T	ENSP00000344546.5:p.Arg1185Ter
ENST00000350026.10:c.3265C>T	ENSP00000055163.7:p.Arg1089Ter
ENST00000414678.7:c.1831C>T	ENSP00000412835.2:p.Arg611Ter
ENST00000635849.1:c.994C>T	ENSP00000490948.1:p.Arg332Ter
ENST00000635957.1:c.628C>T	ENSP00000490385.1:p.Arg210Ter
ENST00000636930.2:c.3673C>T MANE Select	ENSP00000490491.2:p.Arg1225Ter
ENST00000636940.1:n.1670C>T
ENST00000637015.1:c.1041C>T
ENST00000637568.1:c.955C>T
ENST00000637741.1:n.339C>T
ENST00000637810.1:c.1015C>T	ENSP00000489636.1:p.Arg339Ter
ENST00000637904.1:c.1174C>T	ENSP00000490550.1:p.Arg392Ter
ENST00000647938.1:c.3304C>T	ENSP00000498155.1:p.Arg1102Ter
ENST00000319584.10:c.1690C>T	ENSP00000313006.6:p.Arg564Ter
ENST00000346085.9:c.3304C>T	ENSP00000344546.4:p.Arg1102Ter
ENST00000350026.9:c.3265C>T	ENSP00000055163.7:p.Arg1089Ter
ENST00000400790.3:c.466C>T	ENSP00000383596.3:p.Arg156Ter
ENST00000414678.6:c.1831C>T	ENSP00000412835.2:p.Arg611Ter
ENST00000478761.3:c.875C>T
NM_017519.2:c.3265C>T	NP_059989.2:p.Arg1089Ter
NM_020732.3:c.3304C>T	NP_065783.3:p.Arg1102Ter
XM_005267069.3:c.3424C>T	XP_005267126.2:p.Arg1142Ter
XM_011535984.1:c.2503C>T	XP_011534286.1:p.Arg835Ter
XM_011535985.1:c.2323C>T	XP_011534287.1:p.Arg775Ter
XM_011535986.1:c.2083C>T	XP_011534288.1:p.Arg695Ter
XM_011535987.1:c.1702C>T	XP_011534289.1:p.Arg568Ter
XM_011535988.1:c.565C>T	XP_011534290.1:p.Arg189Ter
NM_001346813.1:c.3424C>T	NP_001333742.1:p.Arg1142Ter
NM_001363725.1:c.1174C>T	NP_001350654.1:p.Arg392Ter
XM_011535984.2:c.3634C>T	XP_011534286.2:p.Arg1212Ter
XM_011535988.3:c.565C>T	XP_011534290.1:p.Arg189Ter
XM_017011103.2:c.3535C>T	XP_016866592.1:p.Arg1179Ter
XM_017011104.1:c.3505C>T	XP_016866593.1:p.Arg1169Ter
XM_017011105.2:c.3475C>T	XP_016866594.1:p.Arg1159Ter
XM_017011106.2:c.3346C>T	XP_016866595.1:p.Arg1116Ter
XM_017011107.2:c.3325C>T	XP_016866596.1:p.Arg1109Ter
XR_002956289.1:n.3717C>T
NM_001363725.2:c.1174C>T	NP_001350654.1:p.Arg392Ter
NM_001371656.1:c.3553C>T	NP_001358585.1:p.Arg1185Ter
NM_001374820.1:c.3553C>T	NP_001361749.1:p.Arg1185Ter
NM_001374828.1:c.3673C>T MANE Select	NP_001361757.1:p.Arg1225Ter
NM_017519.3:c.3514C>T	NP_059989.3:p.Arg1172Ter