Canonical Allele Identifier: CA366241859

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 2167313
• ClinVar RCV Id: RCV003092090
• dbSNP Id: rs2128374412
• gnomAD v4: 6-157201077-C-T
• COSMIC: COSM1441823 ; COSM1441824
• MyVariant Identifiers: chr6:g.157522211C>T (hg19) ; chr6:g.157201077C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201077C>T , CM000668.2:g.157201077C>T	GRCh38
NC_000006.11:g.157522211C>T , CM000668.1:g.157522211C>T	GRCh37
NC_000006.10:g.157563903C>T	NCBI36
NG_032093.1:g.428148C>T
NG_032093.2:g.428148C>T
NG_066624.1:g.430052C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4693C>T	ENSP00000055163.8:p.Arg1565Cys
ENST00000414678.8:c.4762C>T	ENSP00000412835.3:p.Arg1588Cys
ENST00000637015.2:c.4981C>T	ENSP00000489729.2:p.Arg1661Cys
ENST00000346085.10:c.4732C>T	ENSP00000344546.5:p.Arg1578Cys
ENST00000350026.10:c.4444C>T	ENSP00000055163.7:p.Arg1482Cys
ENST00000414678.7:c.3010C>T	ENSP00000412835.2:p.Arg1004Cys
ENST00000635849.1:c.2173C>T	ENSP00000490948.1:p.Arg725Cys
ENST00000635957.1:c.1804C>T	ENSP00000490385.1:p.Arg602Cys
ENST00000636227.1:n.3315C>T
ENST00000636254.1:n.772C>T
ENST00000636930.2:c.4852C>T MANE Select	ENSP00000490491.2:p.Arg1618Cys
ENST00000636940.1:n.2849C>T
ENST00000637015.1:c.2220C>T
ENST00000637568.1:c.2134C>T
ENST00000637741.1:n.1518C>T
ENST00000637810.1:c.2194C>T	ENSP00000489636.1:p.Arg732Cys
ENST00000637904.1:c.2353C>T	ENSP00000490550.1:p.Arg785Cys
ENST00000647938.1:c.4483C>T	ENSP00000498155.1:p.Arg1495Cys
ENST00000346085.9:c.4483C>T	ENSP00000344546.4:p.Arg1495Cys
ENST00000350026.9:c.4444C>T	ENSP00000055163.7:p.Arg1482Cys
ENST00000414678.6:c.3010C>T	ENSP00000412835.2:p.Arg1004Cys
NM_017519.2:c.4444C>T	NP_059989.2:p.Arg1482Cys
NM_020732.3:c.4483C>T	NP_065783.3:p.Arg1495Cys
XM_005267069.3:c.4603C>T	XP_005267126.2:p.Arg1535Cys
XM_011535984.1:c.3682C>T	XP_011534286.1:p.Arg1228Cys
XM_011535985.1:c.3502C>T	XP_011534287.1:p.Arg1168Cys
XM_011535986.1:c.3262C>T	XP_011534288.1:p.Arg1088Cys
XM_011535987.1:c.2881C>T	XP_011534289.1:p.Arg961Cys
XM_011535988.1:c.1744C>T	XP_011534290.1:p.Arg582Cys
NM_001346813.1:c.4603C>T	NP_001333742.1:p.Arg1535Cys
NM_001363725.1:c.2353C>T	NP_001350654.1:p.Arg785Cys
XM_011535984.2:c.4813C>T	XP_011534286.2:p.Arg1605Cys
XM_011535988.3:c.1744C>T	XP_011534290.1:p.Arg582Cys
XM_017011103.2:c.4714C>T	XP_016866592.1:p.Arg1572Cys
XM_017011104.1:c.4684C>T	XP_016866593.1:p.Arg1562Cys
XM_017011105.2:c.4654C>T	XP_016866594.1:p.Arg1552Cys
XM_017011106.2:c.4525C>T	XP_016866595.1:p.Arg1509Cys
XM_017011107.2:c.4504C>T	XP_016866596.1:p.Arg1502Cys
XR_002956289.1:n.4799C>T
NM_001363725.2:c.2353C>T	NP_001350654.1:p.Arg785Cys
NM_001371656.1:c.4732C>T	NP_001358585.1:p.Arg1578Cys
NM_001374820.1:c.4732C>T	NP_001361749.1:p.Arg1578Cys
NM_001374828.1:c.4852C>T MANE Select	NP_001361757.1:p.Arg1618Cys
NM_017519.3:c.4693C>T	NP_059989.3:p.Arg1565Cys