Canonical Allele Identifier: CA366239847

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366590
• MyVariant Identifiers: chr6:g.157520024C>G (hg19) ; chr6:g.157198890C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198890C>G , CM000668.2:g.157198890C>G	GRCh38
NC_000006.11:g.157520024C>G , CM000668.1:g.157520024C>G	GRCh37
NC_000006.10:g.157561716C>G	NCBI36
NG_032093.1:g.425961C>G
NG_032093.2:g.425961C>G
NG_066624.1:g.427865C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4303C>G	ENSP00000055163.8:p.Leu1435Val
ENST00000414678.8:c.4372C>G	ENSP00000412835.3:p.Leu1458Val
ENST00000637015.2:c.4591C>G	ENSP00000489729.2:p.Leu1531Val
ENST00000346085.10:c.4342C>G	ENSP00000344546.5:p.Leu1448Val
ENST00000350026.10:c.4054C>G	ENSP00000055163.7:p.Leu1352Val
ENST00000414678.7:c.2620C>G	ENSP00000412835.2:p.Leu874Val
ENST00000635849.1:c.1783C>G	ENSP00000490948.1:p.Leu595Val
ENST00000635957.1:c.1414C>G	ENSP00000490385.1:p.Leu472Val
ENST00000636227.1:n.2925C>G
ENST00000636254.1:n.382C>G
ENST00000636930.2:c.4462C>G MANE Select	ENSP00000490491.2:p.Leu1488Val
ENST00000636940.1:n.2459C>G
ENST00000637015.1:c.1830C>G
ENST00000637568.1:c.1744C>G
ENST00000637741.1:n.1128C>G
ENST00000637810.1:c.1804C>G	ENSP00000489636.1:p.Leu602Val
ENST00000637904.1:c.1963C>G	ENSP00000490550.1:p.Leu655Val
ENST00000647938.1:c.4093C>G	ENSP00000498155.1:p.Leu1365Val
ENST00000346085.9:c.4093C>G	ENSP00000344546.4:p.Leu1365Val
ENST00000350026.9:c.4054C>G	ENSP00000055163.7:p.Leu1352Val
ENST00000414678.6:c.2620C>G	ENSP00000412835.2:p.Leu874Val
NM_017519.2:c.4054C>G	NP_059989.2:p.Leu1352Val
NM_020732.3:c.4093C>G	NP_065783.3:p.Leu1365Val
XM_005267069.3:c.4213C>G	XP_005267126.2:p.Leu1405Val
XM_011535984.1:c.3292C>G	XP_011534286.1:p.Leu1098Val
XM_011535985.1:c.3112C>G	XP_011534287.1:p.Leu1038Val
XM_011535986.1:c.2872C>G	XP_011534288.1:p.Leu958Val
XM_011535987.1:c.2491C>G	XP_011534289.1:p.Leu831Val
XM_011535988.1:c.1354C>G	XP_011534290.1:p.Leu452Val
NM_001346813.1:c.4213C>G	NP_001333742.1:p.Leu1405Val
NM_001363725.1:c.1963C>G	NP_001350654.1:p.Leu655Val
XM_011535984.2:c.4423C>G	XP_011534286.2:p.Leu1475Val
XM_011535988.3:c.1354C>G	XP_011534290.1:p.Leu452Val
XM_017011103.2:c.4324C>G	XP_016866592.1:p.Leu1442Val
XM_017011104.1:c.4294C>G	XP_016866593.1:p.Leu1432Val
XM_017011105.2:c.4264C>G	XP_016866594.1:p.Leu1422Val
XM_017011106.2:c.4135C>G	XP_016866595.1:p.Leu1379Val
XM_017011107.2:c.4114C>G	XP_016866596.1:p.Leu1372Val
XR_002956289.1:n.4427-1815C>G
NM_001363725.2:c.1963C>G	NP_001350654.1:p.Leu655Val
NM_001371656.1:c.4342C>G	NP_001358585.1:p.Leu1448Val
NM_001374820.1:c.4342C>G	NP_001361749.1:p.Leu1448Val
NM_001374828.1:c.4462C>G MANE Select	NP_001361757.1:p.Leu1488Val
NM_017519.3:c.4303C>G	NP_059989.3:p.Leu1435Val