Canonical Allele Identifier: CA203785

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 199160
• ClinVar RCV Id: RCV000358610 ; RCV001330749 ; RCV001533110 ; RCV001291271
• dbSNP Id: rs794727977
• MyVariant Identifiers: chr6:g.157469898C>T (hg19) ; chr6:g.157148764C>T (hg38)
• PubMed: PMID:26785492

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148764C>T , CM000668.2:g.157148764C>T	GRCh38
NC_000006.11:g.157469898C>T , CM000668.1:g.157469898C>T	GRCh37
NC_000006.10:g.157511590C>T	NCBI36
NG_032093.1:g.375835C>T
NG_032093.2:g.375835C>T
NG_066624.1:g.377739C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2902C>T	ENSP00000055163.8:p.Arg968Ter
ENST00000414678.8:c.2812C>T	ENSP00000412835.3:p.Arg938Ter
ENST00000637015.2:c.2902C>T	ENSP00000489729.2:p.Arg968Ter
ENST00000319584.11:c.916C>T	ENSP00000313006.7:p.Arg306Ter
ENST00000346085.10:c.2941C>T	ENSP00000344546.5:p.Arg981Ter
ENST00000350026.10:c.2653C>T	ENSP00000055163.7:p.Arg885Ter
ENST00000414678.7:c.1060C>T	ENSP00000412835.2:p.Arg354Ter
ENST00000452544.2:n.803C>T
ENST00000635849.1:c.223C>T	ENSP00000490948.1:p.Arg75Ter
ENST00000636426.1:n.36C>T
ENST00000636930.2:c.2902C>T MANE Select	ENSP00000490491.2:p.Arg968Ter
ENST00000637015.1:c.141C>T
ENST00000637810.1:c.403C>T	ENSP00000489636.1:p.Arg135Ter
ENST00000637904.1:c.403C>T	ENSP00000490550.1:p.Arg135Ter
ENST00000647938.1:c.2692C>T	ENSP00000498155.1:p.Arg898Ter
ENST00000674190.1:n.1651C>T
ENST00000319584.10:c.919C>T	ENSP00000313006.6:p.Arg307Ter
ENST00000346085.9:c.2692C>T	ENSP00000344546.4:p.Arg898Ter
ENST00000350026.9:c.2653C>T	ENSP00000055163.7:p.Arg885Ter
ENST00000414678.6:c.1060C>T	ENSP00000412835.2:p.Arg354Ter
ENST00000452544.1:n.749C>T
NM_017519.2:c.2653C>T	NP_059989.2:p.Arg885Ter
NM_020732.3:c.2692C>T	NP_065783.3:p.Arg898Ter
XM_005267069.3:c.2653C>T	XP_005267126.2:p.Arg885Ter
XM_011535984.1:c.1603C>T	XP_011534286.1:p.Arg535Ter
XM_011535985.1:c.1423C>T	XP_011534287.1:p.Arg475Ter
XM_011535986.1:c.1183C>T	XP_011534288.1:p.Arg395Ter
XM_011535987.1:c.802C>T	XP_011534289.1:p.Arg268Ter
XM_011535988.1:c.-20+15557C>T	XP_011534290.1:n.-20+15557C>T
NM_001346813.1:c.2653C>T	NP_001333742.1:p.Arg885Ter
NM_001363725.1:c.403C>T	NP_001350654.1:p.Arg135Ter
XM_011535984.2:c.2734C>T	XP_011534286.2:p.Arg912Ter
XM_011535988.3:c.-20+15557C>T	XP_011534290.1:n.-20+15557C>T
XM_017011103.2:c.2734C>T	XP_016866592.1:p.Arg912Ter
XM_017011104.1:c.2734C>T	XP_016866593.1:p.Arg912Ter
XM_017011105.2:c.2734C>T	XP_016866594.1:p.Arg912Ter
XM_017011106.2:c.2734C>T	XP_016866595.1:p.Arg912Ter
XM_017011107.2:c.2554C>T	XP_016866596.1:p.Arg852Ter
XR_002956289.1:n.2817C>T
NM_001363725.2:c.403C>T	NP_001350654.1:p.Arg135Ter
NM_001371656.1:c.2941C>T	NP_001358585.1:p.Arg981Ter
NM_001374820.1:c.2941C>T	NP_001361749.1:p.Arg981Ter
NM_001374828.1:c.2902C>T MANE Select	NP_001361757.1:p.Arg968Ter
NM_017519.3:c.2902C>T	NP_059989.3:p.Arg968Ter