Canonical Allele Identifier: CA366234806

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511192A>T (hg19) ; chr6:g.157190058A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190058A>T , CM000668.2:g.157190058A>T	GRCh38
NC_000006.11:g.157511192A>T , CM000668.1:g.157511192A>T	GRCh37
NC_000006.10:g.157552884A>T	NCBI36
NG_032093.1:g.417129A>T
NG_032093.2:g.417129A>T
NG_066624.1:g.419033A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3920A>T	ENSP00000055163.8:p.His1307Leu
ENST00000414678.8:c.3989A>T	ENSP00000412835.3:p.His1330Leu
ENST00000637015.2:c.4208A>T	ENSP00000489729.2:p.His1403Leu
ENST00000346085.10:c.3959A>T	ENSP00000344546.5:p.His1320Leu
ENST00000350026.10:c.3671A>T	ENSP00000055163.7:p.His1224Leu
ENST00000414678.7:c.2237A>T	ENSP00000412835.2:p.His746Leu
ENST00000635849.1:c.1400A>T	ENSP00000490948.1:p.His467Leu
ENST00000635957.1:c.1031A>T	ENSP00000490385.1:p.His344Leu
ENST00000636930.2:c.4079A>T MANE Select	ENSP00000490491.2:p.His1360Leu
ENST00000636940.1:n.2076A>T
ENST00000637015.1:c.1447A>T
ENST00000637568.1:c.1361A>T
ENST00000637741.1:n.745A>T
ENST00000637810.1:c.1421A>T	ENSP00000489636.1:p.His474Leu
ENST00000637904.1:c.1580A>T	ENSP00000490550.1:p.His527Leu
ENST00000647938.1:c.3710A>T	ENSP00000498155.1:p.His1237Leu
ENST00000346085.9:c.3710A>T	ENSP00000344546.4:p.His1237Leu
ENST00000350026.9:c.3671A>T	ENSP00000055163.7:p.His1224Leu
ENST00000414678.6:c.2237A>T	ENSP00000412835.2:p.His746Leu
NM_017519.2:c.3671A>T	NP_059989.2:p.His1224Leu
NM_020732.3:c.3710A>T	NP_065783.3:p.His1237Leu
XM_005267069.3:c.3830A>T	XP_005267126.2:p.His1277Leu
XM_011535984.1:c.2909A>T	XP_011534286.1:p.His970Leu
XM_011535985.1:c.2729A>T	XP_011534287.1:p.His910Leu
XM_011535986.1:c.2489A>T	XP_011534288.1:p.His830Leu
XM_011535987.1:c.2108A>T	XP_011534289.1:p.His703Leu
XM_011535988.1:c.971A>T	XP_011534290.1:p.His324Leu
NM_001346813.1:c.3830A>T	NP_001333742.1:p.His1277Leu
NM_001363725.1:c.1580A>T	NP_001350654.1:p.His527Leu
XM_011535984.2:c.4040A>T	XP_011534286.2:p.His1347Leu
XM_011535988.3:c.971A>T	XP_011534290.1:p.His324Leu
XM_017011103.2:c.3941A>T	XP_016866592.1:p.His1314Leu
XM_017011104.1:c.3911A>T	XP_016866593.1:p.His1304Leu
XM_017011105.2:c.3881A>T	XP_016866594.1:p.His1294Leu
XM_017011106.2:c.3752A>T	XP_016866595.1:p.His1251Leu
XM_017011107.2:c.3731A>T	XP_016866596.1:p.His1244Leu
XR_002956289.1:n.4123A>T
NM_001363725.2:c.1580A>T	NP_001350654.1:p.His527Leu
NM_001371656.1:c.3959A>T	NP_001358585.1:p.His1320Leu
NM_001374820.1:c.3959A>T	NP_001361749.1:p.His1320Leu
NM_001374828.1:c.4079A>T MANE Select	NP_001361757.1:p.His1360Leu
NM_017519.3:c.3920A>T	NP_059989.3:p.His1307Leu