Canonical Allele Identifier: CA366234751

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511188G>T (hg19) ; chr6:g.157190054G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190054G>T , CM000668.2:g.157190054G>T	GRCh38
NC_000006.11:g.157511188G>T , CM000668.1:g.157511188G>T	GRCh37
NC_000006.10:g.157552880G>T	NCBI36
NG_032093.1:g.417125G>T
NG_032093.2:g.417125G>T
NG_066624.1:g.419029G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3916G>T	ENSP00000055163.8:p.Val1306Leu
ENST00000414678.8:c.3985G>T	ENSP00000412835.3:p.Val1329Leu
ENST00000637015.2:c.4204G>T	ENSP00000489729.2:p.Val1402Leu
ENST00000346085.10:c.3955G>T	ENSP00000344546.5:p.Val1319Leu
ENST00000350026.10:c.3667G>T	ENSP00000055163.7:p.Val1223Leu
ENST00000414678.7:c.2233G>T	ENSP00000412835.2:p.Val745Leu
ENST00000635849.1:c.1396G>T	ENSP00000490948.1:p.Val466Leu
ENST00000635957.1:c.1027G>T	ENSP00000490385.1:p.Val343Leu
ENST00000636930.2:c.4075G>T MANE Select	ENSP00000490491.2:p.Val1359Leu
ENST00000636940.1:n.2072G>T
ENST00000637015.1:c.1443G>T
ENST00000637568.1:c.1357G>T
ENST00000637741.1:n.741G>T
ENST00000637810.1:c.1417G>T	ENSP00000489636.1:p.Val473Leu
ENST00000637904.1:c.1576G>T	ENSP00000490550.1:p.Val526Leu
ENST00000647938.1:c.3706G>T	ENSP00000498155.1:p.Val1236Leu
ENST00000346085.9:c.3706G>T	ENSP00000344546.4:p.Val1236Leu
ENST00000350026.9:c.3667G>T	ENSP00000055163.7:p.Val1223Leu
ENST00000414678.6:c.2233G>T	ENSP00000412835.2:p.Val745Leu
NM_017519.2:c.3667G>T	NP_059989.2:p.Val1223Leu
NM_020732.3:c.3706G>T	NP_065783.3:p.Val1236Leu
XM_005267069.3:c.3826G>T	XP_005267126.2:p.Val1276Leu
XM_011535984.1:c.2905G>T	XP_011534286.1:p.Val969Leu
XM_011535985.1:c.2725G>T	XP_011534287.1:p.Val909Leu
XM_011535986.1:c.2485G>T	XP_011534288.1:p.Val829Leu
XM_011535987.1:c.2104G>T	XP_011534289.1:p.Val702Leu
XM_011535988.1:c.967G>T	XP_011534290.1:p.Val323Leu
NM_001346813.1:c.3826G>T	NP_001333742.1:p.Val1276Leu
NM_001363725.1:c.1576G>T	NP_001350654.1:p.Val526Leu
XM_011535984.2:c.4036G>T	XP_011534286.2:p.Val1346Leu
XM_011535988.3:c.967G>T	XP_011534290.1:p.Val323Leu
XM_017011103.2:c.3937G>T	XP_016866592.1:p.Val1313Leu
XM_017011104.1:c.3907G>T	XP_016866593.1:p.Val1303Leu
XM_017011105.2:c.3877G>T	XP_016866594.1:p.Val1293Leu
XM_017011106.2:c.3748G>T	XP_016866595.1:p.Val1250Leu
XM_017011107.2:c.3727G>T	XP_016866596.1:p.Val1243Leu
XR_002956289.1:n.4119G>T
NM_001363725.2:c.1576G>T	NP_001350654.1:p.Val526Leu
NM_001371656.1:c.3955G>T	NP_001358585.1:p.Val1319Leu
NM_001374820.1:c.3955G>T	NP_001361749.1:p.Val1319Leu
NM_001374828.1:c.4075G>T MANE Select	NP_001361757.1:p.Val1359Leu
NM_017519.3:c.3916G>T	NP_059989.3:p.Val1306Leu