Canonical Allele Identifier: CA366242332

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522384G>C (hg19) ; chr6:g.157201250G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201250G>C , CM000668.2:g.157201250G>C	GRCh38
NC_000006.11:g.157522384G>C , CM000668.1:g.157522384G>C	GRCh37
NC_000006.10:g.157564076G>C	NCBI36
NG_032093.1:g.428321G>C
NG_032093.2:g.428321G>C
NG_066624.1:g.430225G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4866G>C	ENSP00000055163.8:p.Arg1622Ser
ENST00000414678.8:c.4935G>C	ENSP00000412835.3:p.Arg1645Ser
ENST00000637015.2:c.5154G>C	ENSP00000489729.2:p.Arg1718Ser
ENST00000346085.10:c.4905G>C	ENSP00000344546.5:p.Arg1635Ser
ENST00000350026.10:c.4617G>C	ENSP00000055163.7:p.Arg1539Ser
ENST00000414678.7:c.3183G>C	ENSP00000412835.2:p.Arg1061Ser
ENST00000635849.1:c.2346G>C	ENSP00000490948.1:p.Arg782Ser
ENST00000635957.1:c.1977G>C	ENSP00000490385.1:p.Arg659Ser
ENST00000636227.1:n.3488G>C
ENST00000636254.1:n.945G>C
ENST00000636930.2:c.5025G>C MANE Select	ENSP00000490491.2:p.Arg1675Ser
ENST00000636940.1:n.3022G>C
ENST00000637015.1:c.2393G>C
ENST00000637568.1:c.2307G>C
ENST00000637741.1:n.1691G>C
ENST00000637810.1:c.2367G>C	ENSP00000489636.1:p.Arg789Ser
ENST00000637904.1:c.2526G>C	ENSP00000490550.1:p.Arg842Ser
ENST00000647938.1:c.4656G>C	ENSP00000498155.1:p.Arg1552Ser
ENST00000346085.9:c.4656G>C	ENSP00000344546.4:p.Arg1552Ser
ENST00000350026.9:c.4617G>C	ENSP00000055163.7:p.Arg1539Ser
ENST00000414678.6:c.3183G>C	ENSP00000412835.2:p.Arg1061Ser
NM_017519.2:c.4617G>C	NP_059989.2:p.Arg1539Ser
NM_020732.3:c.4656G>C	NP_065783.3:p.Arg1552Ser
XM_005267069.3:c.4776G>C	XP_005267126.2:p.Arg1592Ser
XM_011535984.1:c.3855G>C	XP_011534286.1:p.Arg1285Ser
XM_011535985.1:c.3675G>C	XP_011534287.1:p.Arg1225Ser
XM_011535986.1:c.3435G>C	XP_011534288.1:p.Arg1145Ser
XM_011535987.1:c.3054G>C	XP_011534289.1:p.Arg1018Ser
XM_011535988.1:c.1917G>C	XP_011534290.1:p.Arg639Ser
NM_001346813.1:c.4776G>C	NP_001333742.1:p.Arg1592Ser
NM_001363725.1:c.2526G>C	NP_001350654.1:p.Arg842Ser
XM_011535984.2:c.4986G>C	XP_011534286.2:p.Arg1662Ser
XM_011535988.3:c.1917G>C	XP_011534290.1:p.Arg639Ser
XM_017011103.2:c.4887G>C	XP_016866592.1:p.Arg1629Ser
XM_017011104.1:c.4857G>C	XP_016866593.1:p.Arg1619Ser
XM_017011105.2:c.4827G>C	XP_016866594.1:p.Arg1609Ser
XM_017011106.2:c.4698G>C	XP_016866595.1:p.Arg1566Ser
XM_017011107.2:c.4677G>C	XP_016866596.1:p.Arg1559Ser
XR_002956289.1:n.4972G>C
NM_001363725.2:c.2526G>C	NP_001350654.1:p.Arg842Ser
NM_001371656.1:c.4905G>C	NP_001358585.1:p.Arg1635Ser
NM_001374820.1:c.4905G>C	NP_001361749.1:p.Arg1635Ser
NM_001374828.1:c.5025G>C MANE Select	NP_001361757.1:p.Arg1675Ser
NM_017519.3:c.4866G>C	NP_059989.3:p.Arg1622Ser