Canonical Allele Identifier: CA366242705

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522487G>T (hg19) ; chr6:g.157201353G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201353G>T , CM000668.2:g.157201353G>T	GRCh38
NC_000006.11:g.157522487G>T , CM000668.1:g.157522487G>T	GRCh37
NC_000006.10:g.157564179G>T	NCBI36
NG_032093.1:g.428424G>T
NG_032093.2:g.428424G>T
NG_066624.1:g.430328G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4969G>T	ENSP00000055163.8:p.Val1657Phe
ENST00000414678.8:c.5038G>T	ENSP00000412835.3:p.Val1680Phe
ENST00000637015.2:c.5257G>T	ENSP00000489729.2:p.Val1753Phe
ENST00000346085.10:c.5008G>T	ENSP00000344546.5:p.Val1670Phe
ENST00000350026.10:c.4720G>T	ENSP00000055163.7:p.Val1574Phe
ENST00000414678.7:c.3286G>T	ENSP00000412835.2:p.Val1096Phe
ENST00000635849.1:c.2449G>T	ENSP00000490948.1:p.Val817Phe
ENST00000635957.1:c.2080G>T	ENSP00000490385.1:p.Val694Phe
ENST00000636227.1:n.3591G>T
ENST00000636254.1:n.1048G>T
ENST00000636930.2:c.5128G>T MANE Select	ENSP00000490491.2:p.Val1710Phe
ENST00000636940.1:n.3125G>T
ENST00000637015.1:c.2496G>T
ENST00000637568.1:c.2410G>T
ENST00000637741.1:n.1794G>T
ENST00000637810.1:c.2470G>T	ENSP00000489636.1:p.Val824Phe
ENST00000637904.1:c.2629G>T	ENSP00000490550.1:p.Val877Phe
ENST00000647938.1:c.4759G>T	ENSP00000498155.1:p.Val1587Phe
ENST00000346085.9:c.4759G>T	ENSP00000344546.4:p.Val1587Phe
ENST00000350026.9:c.4720G>T	ENSP00000055163.7:p.Val1574Phe
ENST00000414678.6:c.3286G>T	ENSP00000412835.2:p.Val1096Phe
NM_017519.2:c.4720G>T	NP_059989.2:p.Val1574Phe
NM_020732.3:c.4759G>T	NP_065783.3:p.Val1587Phe
XM_005267069.3:c.4879G>T	XP_005267126.2:p.Val1627Phe
XM_011535984.1:c.3958G>T	XP_011534286.1:p.Val1320Phe
XM_011535985.1:c.3778G>T	XP_011534287.1:p.Val1260Phe
XM_011535986.1:c.3538G>T	XP_011534288.1:p.Val1180Phe
XM_011535987.1:c.3157G>T	XP_011534289.1:p.Val1053Phe
XM_011535988.1:c.2020G>T	XP_011534290.1:p.Val674Phe
NM_001346813.1:c.4879G>T	NP_001333742.1:p.Val1627Phe
NM_001363725.1:c.2629G>T	NP_001350654.1:p.Val877Phe
XM_011535984.2:c.5089G>T	XP_011534286.2:p.Val1697Phe
XM_011535988.3:c.2020G>T	XP_011534290.1:p.Val674Phe
XM_017011103.2:c.4990G>T	XP_016866592.1:p.Val1664Phe
XM_017011104.1:c.4960G>T	XP_016866593.1:p.Val1654Phe
XM_017011105.2:c.4930G>T	XP_016866594.1:p.Val1644Phe
XM_017011106.2:c.4801G>T	XP_016866595.1:p.Val1601Phe
XM_017011107.2:c.4780G>T	XP_016866596.1:p.Val1594Phe
XR_002956289.1:n.5075G>T
NM_001363725.2:c.2629G>T	NP_001350654.1:p.Val877Phe
NM_001371656.1:c.5008G>T	NP_001358585.1:p.Val1670Phe
NM_001374820.1:c.5008G>T	NP_001361749.1:p.Val1670Phe
NM_001374828.1:c.5128G>T MANE Select	NP_001361757.1:p.Val1710Phe
NM_017519.3:c.4969G>T	NP_059989.3:p.Val1657Phe