Canonical Allele Identifier: CA366242590

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522467T>G (hg19) ; chr6:g.157201333T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201333T>G , CM000668.2:g.157201333T>G	GRCh38
NC_000006.11:g.157522467T>G , CM000668.1:g.157522467T>G	GRCh37
NC_000006.10:g.157564159T>G	NCBI36
NG_032093.1:g.428404T>G
NG_032093.2:g.428404T>G
NG_066624.1:g.430308T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4949T>G	ENSP00000055163.8:p.Met1650Arg
ENST00000414678.8:c.5018T>G	ENSP00000412835.3:p.Met1673Arg
ENST00000637015.2:c.5237T>G	ENSP00000489729.2:p.Met1746Arg
ENST00000346085.10:c.4988T>G	ENSP00000344546.5:p.Met1663Arg
ENST00000350026.10:c.4700T>G	ENSP00000055163.7:p.Met1567Arg
ENST00000414678.7:c.3266T>G	ENSP00000412835.2:p.Met1089Arg
ENST00000635849.1:c.2429T>G	ENSP00000490948.1:p.Met810Arg
ENST00000635957.1:c.2060T>G	ENSP00000490385.1:p.Met687Arg
ENST00000636227.1:n.3571T>G
ENST00000636254.1:n.1028T>G
ENST00000636930.2:c.5108T>G MANE Select	ENSP00000490491.2:p.Met1703Arg
ENST00000636940.1:n.3105T>G
ENST00000637015.1:c.2476T>G
ENST00000637568.1:c.2390T>G
ENST00000637741.1:n.1774T>G
ENST00000637810.1:c.2450T>G	ENSP00000489636.1:p.Met817Arg
ENST00000637904.1:c.2609T>G	ENSP00000490550.1:p.Met870Arg
ENST00000647938.1:c.4739T>G	ENSP00000498155.1:p.Met1580Arg
ENST00000346085.9:c.4739T>G	ENSP00000344546.4:p.Met1580Arg
ENST00000350026.9:c.4700T>G	ENSP00000055163.7:p.Met1567Arg
ENST00000414678.6:c.3266T>G	ENSP00000412835.2:p.Met1089Arg
NM_017519.2:c.4700T>G	NP_059989.2:p.Met1567Arg
NM_020732.3:c.4739T>G	NP_065783.3:p.Met1580Arg
XM_005267069.3:c.4859T>G	XP_005267126.2:p.Met1620Arg
XM_011535984.1:c.3938T>G	XP_011534286.1:p.Met1313Arg
XM_011535985.1:c.3758T>G	XP_011534287.1:p.Met1253Arg
XM_011535986.1:c.3518T>G	XP_011534288.1:p.Met1173Arg
XM_011535987.1:c.3137T>G	XP_011534289.1:p.Met1046Arg
XM_011535988.1:c.2000T>G	XP_011534290.1:p.Met667Arg
NM_001346813.1:c.4859T>G	NP_001333742.1:p.Met1620Arg
NM_001363725.1:c.2609T>G	NP_001350654.1:p.Met870Arg
XM_011535984.2:c.5069T>G	XP_011534286.2:p.Met1690Arg
XM_011535988.3:c.2000T>G	XP_011534290.1:p.Met667Arg
XM_017011103.2:c.4970T>G	XP_016866592.1:p.Met1657Arg
XM_017011104.1:c.4940T>G	XP_016866593.1:p.Met1647Arg
XM_017011105.2:c.4910T>G	XP_016866594.1:p.Met1637Arg
XM_017011106.2:c.4781T>G	XP_016866595.1:p.Met1594Arg
XM_017011107.2:c.4760T>G	XP_016866596.1:p.Met1587Arg
XR_002956289.1:n.5055T>G
NM_001363725.2:c.2609T>G	NP_001350654.1:p.Met870Arg
NM_001371656.1:c.4988T>G	NP_001358585.1:p.Met1663Arg
NM_001374820.1:c.4988T>G	NP_001361749.1:p.Met1663Arg
NM_001374828.1:c.5108T>G MANE Select	NP_001361757.1:p.Met1703Arg
NM_017519.3:c.4949T>G	NP_059989.3:p.Met1650Arg