Canonical Allele Identifier: CA366234914

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511201T>C (hg19) ; chr6:g.157190067T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190067T>C , CM000668.2:g.157190067T>C	GRCh38
NC_000006.11:g.157511201T>C , CM000668.1:g.157511201T>C	GRCh37
NC_000006.10:g.157552893T>C	NCBI36
NG_032093.1:g.417138T>C
NG_032093.2:g.417138T>C
NG_066624.1:g.419042T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3929T>C	ENSP00000055163.8:p.Phe1310Ser
ENST00000414678.8:c.3998T>C	ENSP00000412835.3:p.Phe1333Ser
ENST00000637015.2:c.4217T>C	ENSP00000489729.2:p.Phe1406Ser
ENST00000346085.10:c.3968T>C	ENSP00000344546.5:p.Phe1323Ser
ENST00000350026.10:c.3680T>C	ENSP00000055163.7:p.Phe1227Ser
ENST00000414678.7:c.2246T>C	ENSP00000412835.2:p.Phe749Ser
ENST00000635849.1:c.1409T>C	ENSP00000490948.1:p.Phe470Ser
ENST00000635957.1:c.1040T>C	ENSP00000490385.1:p.Phe347Ser
ENST00000636930.2:c.4088T>C MANE Select	ENSP00000490491.2:p.Phe1363Ser
ENST00000636940.1:n.2085T>C
ENST00000637015.1:c.1456T>C
ENST00000637568.1:c.1370T>C
ENST00000637741.1:n.754T>C
ENST00000637810.1:c.1430T>C	ENSP00000489636.1:p.Phe477Ser
ENST00000637904.1:c.1589T>C	ENSP00000490550.1:p.Phe530Ser
ENST00000647938.1:c.3719T>C	ENSP00000498155.1:p.Phe1240Ser
ENST00000346085.9:c.3719T>C	ENSP00000344546.4:p.Phe1240Ser
ENST00000350026.9:c.3680T>C	ENSP00000055163.7:p.Phe1227Ser
ENST00000414678.6:c.2246T>C	ENSP00000412835.2:p.Phe749Ser
NM_017519.2:c.3680T>C	NP_059989.2:p.Phe1227Ser
NM_020732.3:c.3719T>C	NP_065783.3:p.Phe1240Ser
XM_005267069.3:c.3839T>C	XP_005267126.2:p.Phe1280Ser
XM_011535984.1:c.2918T>C	XP_011534286.1:p.Phe973Ser
XM_011535985.1:c.2738T>C	XP_011534287.1:p.Phe913Ser
XM_011535986.1:c.2498T>C	XP_011534288.1:p.Phe833Ser
XM_011535987.1:c.2117T>C	XP_011534289.1:p.Phe706Ser
XM_011535988.1:c.980T>C	XP_011534290.1:p.Phe327Ser
NM_001346813.1:c.3839T>C	NP_001333742.1:p.Phe1280Ser
NM_001363725.1:c.1589T>C	NP_001350654.1:p.Phe530Ser
XM_011535984.2:c.4049T>C	XP_011534286.2:p.Phe1350Ser
XM_011535988.3:c.980T>C	XP_011534290.1:p.Phe327Ser
XM_017011103.2:c.3950T>C	XP_016866592.1:p.Phe1317Ser
XM_017011104.1:c.3920T>C	XP_016866593.1:p.Phe1307Ser
XM_017011105.2:c.3890T>C	XP_016866594.1:p.Phe1297Ser
XM_017011106.2:c.3761T>C	XP_016866595.1:p.Phe1254Ser
XM_017011107.2:c.3740T>C	XP_016866596.1:p.Phe1247Ser
XR_002956289.1:n.4132T>C
NM_001363725.2:c.1589T>C	NP_001350654.1:p.Phe530Ser
NM_001371656.1:c.3968T>C	NP_001358585.1:p.Phe1323Ser
NM_001374820.1:c.3968T>C	NP_001361749.1:p.Phe1323Ser
NM_001374828.1:c.4088T>C MANE Select	NP_001361757.1:p.Phe1363Ser
NM_017519.3:c.3929T>C	NP_059989.3:p.Phe1310Ser