Canonical Allele Identifier: CA366241237

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522057C>G (hg19) ; chr6:g.157200923C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200923C>G , CM000668.2:g.157200923C>G	GRCh38
NC_000006.11:g.157522057C>G , CM000668.1:g.157522057C>G	GRCh37
NC_000006.10:g.157563749C>G	NCBI36
NG_032093.1:g.427994C>G
NG_032093.2:g.427994C>G
NG_066624.1:g.429898C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4539C>G	ENSP00000055163.8:p.Ile1513Met
ENST00000414678.8:c.4608C>G	ENSP00000412835.3:p.Ile1536Met
ENST00000637015.2:c.4827C>G	ENSP00000489729.2:p.Ile1609Met
ENST00000346085.10:c.4578C>G	ENSP00000344546.5:p.Ile1526Met
ENST00000350026.10:c.4290C>G	ENSP00000055163.7:p.Ile1430Met
ENST00000414678.7:c.2856C>G	ENSP00000412835.2:p.Ile952Met
ENST00000635849.1:c.2019C>G	ENSP00000490948.1:p.Ile673Met
ENST00000635957.1:c.1650C>G	ENSP00000490385.1:p.Ile550Met
ENST00000636227.1:n.3161C>G
ENST00000636254.1:n.618C>G
ENST00000636930.2:c.4698C>G MANE Select	ENSP00000490491.2:p.Ile1566Met
ENST00000636940.1:n.2695C>G
ENST00000637015.1:c.2066C>G
ENST00000637568.1:c.1980C>G
ENST00000637741.1:n.1364C>G
ENST00000637810.1:c.2040C>G	ENSP00000489636.1:p.Ile680Met
ENST00000637904.1:c.2199C>G	ENSP00000490550.1:p.Ile733Met
ENST00000647938.1:c.4329C>G	ENSP00000498155.1:p.Ile1443Met
ENST00000346085.9:c.4329C>G	ENSP00000344546.4:p.Ile1443Met
ENST00000350026.9:c.4290C>G	ENSP00000055163.7:p.Ile1430Met
ENST00000414678.6:c.2856C>G	ENSP00000412835.2:p.Ile952Met
NM_017519.2:c.4290C>G	NP_059989.2:p.Ile1430Met
NM_020732.3:c.4329C>G	NP_065783.3:p.Ile1443Met
XM_005267069.3:c.4449C>G	XP_005267126.2:p.Ile1483Met
XM_011535984.1:c.3528C>G	XP_011534286.1:p.Ile1176Met
XM_011535985.1:c.3348C>G	XP_011534287.1:p.Ile1116Met
XM_011535986.1:c.3108C>G	XP_011534288.1:p.Ile1036Met
XM_011535987.1:c.2727C>G	XP_011534289.1:p.Ile909Met
XM_011535988.1:c.1590C>G	XP_011534290.1:p.Ile530Met
NM_001346813.1:c.4449C>G	NP_001333742.1:p.Ile1483Met
NM_001363725.1:c.2199C>G	NP_001350654.1:p.Ile733Met
XM_011535984.2:c.4659C>G	XP_011534286.2:p.Ile1553Met
XM_011535988.3:c.1590C>G	XP_011534290.1:p.Ile530Met
XM_017011103.2:c.4560C>G	XP_016866592.1:p.Ile1520Met
XM_017011104.1:c.4530C>G	XP_016866593.1:p.Ile1510Met
XM_017011105.2:c.4500C>G	XP_016866594.1:p.Ile1500Met
XM_017011106.2:c.4371C>G	XP_016866595.1:p.Ile1457Met
XM_017011107.2:c.4350C>G	XP_016866596.1:p.Ile1450Met
XR_002956289.1:n.4645C>G
NM_001363725.2:c.2199C>G	NP_001350654.1:p.Ile733Met
NM_001371656.1:c.4578C>G	NP_001358585.1:p.Ile1526Met
NM_001374820.1:c.4578C>G	NP_001361749.1:p.Ile1526Met
NM_001374828.1:c.4698C>G MANE Select	NP_001361757.1:p.Ile1566Met
NM_017519.3:c.4539C>G	NP_059989.3:p.Ile1513Met