Canonical Allele Identifier: CA366242092

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522274G>C (hg19) ; chr6:g.157201140G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201140G>C , CM000668.2:g.157201140G>C	GRCh38
NC_000006.11:g.157522274G>C , CM000668.1:g.157522274G>C	GRCh37
NC_000006.10:g.157563966G>C	NCBI36
NG_032093.1:g.428211G>C
NG_032093.2:g.428211G>C
NG_066624.1:g.430115G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4756G>C	ENSP00000055163.8:p.Val1586Leu
ENST00000414678.8:c.4825G>C	ENSP00000412835.3:p.Val1609Leu
ENST00000637015.2:c.5044G>C	ENSP00000489729.2:p.Val1682Leu
ENST00000346085.10:c.4795G>C	ENSP00000344546.5:p.Val1599Leu
ENST00000350026.10:c.4507G>C	ENSP00000055163.7:p.Val1503Leu
ENST00000414678.7:c.3073G>C	ENSP00000412835.2:p.Val1025Leu
ENST00000635849.1:c.2236G>C	ENSP00000490948.1:p.Val746Leu
ENST00000635957.1:c.1867G>C	ENSP00000490385.1:p.Val623Leu
ENST00000636227.1:n.3378G>C
ENST00000636254.1:n.835G>C
ENST00000636930.2:c.4915G>C MANE Select	ENSP00000490491.2:p.Val1639Leu
ENST00000636940.1:n.2912G>C
ENST00000637015.1:c.2283G>C
ENST00000637568.1:c.2197G>C
ENST00000637741.1:n.1581G>C
ENST00000637810.1:c.2257G>C	ENSP00000489636.1:p.Val753Leu
ENST00000637904.1:c.2416G>C	ENSP00000490550.1:p.Val806Leu
ENST00000647938.1:c.4546G>C	ENSP00000498155.1:p.Val1516Leu
ENST00000346085.9:c.4546G>C	ENSP00000344546.4:p.Val1516Leu
ENST00000350026.9:c.4507G>C	ENSP00000055163.7:p.Val1503Leu
ENST00000414678.6:c.3073G>C	ENSP00000412835.2:p.Val1025Leu
NM_017519.2:c.4507G>C	NP_059989.2:p.Val1503Leu
NM_020732.3:c.4546G>C	NP_065783.3:p.Val1516Leu
XM_005267069.3:c.4666G>C	XP_005267126.2:p.Val1556Leu
XM_011535984.1:c.3745G>C	XP_011534286.1:p.Val1249Leu
XM_011535985.1:c.3565G>C	XP_011534287.1:p.Val1189Leu
XM_011535986.1:c.3325G>C	XP_011534288.1:p.Val1109Leu
XM_011535987.1:c.2944G>C	XP_011534289.1:p.Val982Leu
XM_011535988.1:c.1807G>C	XP_011534290.1:p.Val603Leu
NM_001346813.1:c.4666G>C	NP_001333742.1:p.Val1556Leu
NM_001363725.1:c.2416G>C	NP_001350654.1:p.Val806Leu
XM_011535984.2:c.4876G>C	XP_011534286.2:p.Val1626Leu
XM_011535988.3:c.1807G>C	XP_011534290.1:p.Val603Leu
XM_017011103.2:c.4777G>C	XP_016866592.1:p.Val1593Leu
XM_017011104.1:c.4747G>C	XP_016866593.1:p.Val1583Leu
XM_017011105.2:c.4717G>C	XP_016866594.1:p.Val1573Leu
XM_017011106.2:c.4588G>C	XP_016866595.1:p.Val1530Leu
XM_017011107.2:c.4567G>C	XP_016866596.1:p.Val1523Leu
XR_002956289.1:n.4862G>C
NM_001363725.2:c.2416G>C	NP_001350654.1:p.Val806Leu
NM_001371656.1:c.4795G>C	NP_001358585.1:p.Val1599Leu
NM_001374820.1:c.4795G>C	NP_001361749.1:p.Val1599Leu
NM_001374828.1:c.4915G>C MANE Select	NP_001361757.1:p.Val1639Leu
NM_017519.3:c.4756G>C	NP_059989.3:p.Val1586Leu