Canonical Allele Identifier: CA366242111

Gene: ARID1B

Linked Data

• dbSNP Id: rs1794081844
• MyVariant Identifiers: chr6:g.157522282G>C (hg19) ; chr6:g.157201148G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201148G>C , CM000668.2:g.157201148G>C	GRCh38
NC_000006.11:g.157522282G>C , CM000668.1:g.157522282G>C	GRCh37
NC_000006.10:g.157563974G>C	NCBI36
NG_032093.1:g.428219G>C
NG_032093.2:g.428219G>C
NG_066624.1:g.430123G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4764G>C	ENSP00000055163.8:p.Gln1588His
ENST00000414678.8:c.4833G>C	ENSP00000412835.3:p.Gln1611His
ENST00000637015.2:c.5052G>C	ENSP00000489729.2:p.Gln1684His
ENST00000346085.10:c.4803G>C	ENSP00000344546.5:p.Gln1601His
ENST00000350026.10:c.4515G>C	ENSP00000055163.7:p.Gln1505His
ENST00000414678.7:c.3081G>C	ENSP00000412835.2:p.Gln1027His
ENST00000635849.1:c.2244G>C	ENSP00000490948.1:p.Gln748His
ENST00000635957.1:c.1875G>C	ENSP00000490385.1:p.Gln625His
ENST00000636227.1:n.3386G>C
ENST00000636254.1:n.843G>C
ENST00000636930.2:c.4923G>C MANE Select	ENSP00000490491.2:p.Gln1641His
ENST00000636940.1:n.2920G>C
ENST00000637015.1:c.2291G>C
ENST00000637568.1:c.2205G>C
ENST00000637741.1:n.1589G>C
ENST00000637810.1:c.2265G>C	ENSP00000489636.1:p.Gln755His
ENST00000637904.1:c.2424G>C	ENSP00000490550.1:p.Gln808His
ENST00000647938.1:c.4554G>C	ENSP00000498155.1:p.Gln1518His
ENST00000346085.9:c.4554G>C	ENSP00000344546.4:p.Gln1518His
ENST00000350026.9:c.4515G>C	ENSP00000055163.7:p.Gln1505His
ENST00000414678.6:c.3081G>C	ENSP00000412835.2:p.Gln1027His
NM_017519.2:c.4515G>C	NP_059989.2:p.Gln1505His
NM_020732.3:c.4554G>C	NP_065783.3:p.Gln1518His
XM_005267069.3:c.4674G>C	XP_005267126.2:p.Gln1558His
XM_011535984.1:c.3753G>C	XP_011534286.1:p.Gln1251His
XM_011535985.1:c.3573G>C	XP_011534287.1:p.Gln1191His
XM_011535986.1:c.3333G>C	XP_011534288.1:p.Gln1111His
XM_011535987.1:c.2952G>C	XP_011534289.1:p.Gln984His
XM_011535988.1:c.1815G>C	XP_011534290.1:p.Gln605His
NM_001346813.1:c.4674G>C	NP_001333742.1:p.Gln1558His
NM_001363725.1:c.2424G>C	NP_001350654.1:p.Gln808His
XM_011535984.2:c.4884G>C	XP_011534286.2:p.Gln1628His
XM_011535988.3:c.1815G>C	XP_011534290.1:p.Gln605His
XM_017011103.2:c.4785G>C	XP_016866592.1:p.Gln1595His
XM_017011104.1:c.4755G>C	XP_016866593.1:p.Gln1585His
XM_017011105.2:c.4725G>C	XP_016866594.1:p.Gln1575His
XM_017011106.2:c.4596G>C	XP_016866595.1:p.Gln1532His
XM_017011107.2:c.4575G>C	XP_016866596.1:p.Gln1525His
XR_002956289.1:n.4870G>C
NM_001363725.2:c.2424G>C	NP_001350654.1:p.Gln808His
NM_001371656.1:c.4803G>C	NP_001358585.1:p.Gln1601His
NM_001374820.1:c.4803G>C	NP_001361749.1:p.Gln1601His
NM_001374828.1:c.4923G>C MANE Select	NP_001361757.1:p.Gln1641His
NM_017519.3:c.4764G>C	NP_059989.3:p.Gln1588His