Canonical Allele Identifier: CA366242591

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4949T>A	ENSP00000055163.8:p.Met1650Lys
ENST00000414678.8:c.5018T>A	ENSP00000412835.3:p.Met1673Lys
ENST00000637015.2:c.5237T>A	ENSP00000489729.2:p.Met1746Lys
ENST00000346085.10:c.4988T>A	ENSP00000344546.5:p.Met1663Lys
ENST00000350026.10:c.4700T>A	ENSP00000055163.7:p.Met1567Lys
ENST00000414678.7:c.3266T>A	ENSP00000412835.2:p.Met1089Lys
ENST00000635849.1:c.2429T>A	ENSP00000490948.1:p.Met810Lys
ENST00000635957.1:c.2060T>A	ENSP00000490385.1:p.Met687Lys
ENST00000636227.1:n.3571T>A
ENST00000636254.1:n.1028T>A
ENST00000636930.2:c.5108T>A MANE Select	ENSP00000490491.2:p.Met1703Lys
ENST00000636940.1:n.3105T>A
ENST00000637015.1:c.2476T>A
ENST00000637568.1:c.2390T>A
ENST00000637741.1:n.1774T>A
ENST00000637810.1:c.2450T>A	ENSP00000489636.1:p.Met817Lys
ENST00000637904.1:c.2609T>A	ENSP00000490550.1:p.Met870Lys
ENST00000647938.1:c.4739T>A	ENSP00000498155.1:p.Met1580Lys
ENST00000346085.9:c.4739T>A	ENSP00000344546.4:p.Met1580Lys
ENST00000350026.9:c.4700T>A	ENSP00000055163.7:p.Met1567Lys
ENST00000414678.6:c.3266T>A	ENSP00000412835.2:p.Met1089Lys
NM_017519.2:c.4700T>A	NP_059989.2:p.Met1567Lys
NM_020732.3:c.4739T>A	NP_065783.3:p.Met1580Lys
XM_005267069.3:c.4859T>A	XP_005267126.2:p.Met1620Lys
XM_011535984.1:c.3938T>A	XP_011534286.1:p.Met1313Lys
XM_011535985.1:c.3758T>A	XP_011534287.1:p.Met1253Lys
XM_011535986.1:c.3518T>A	XP_011534288.1:p.Met1173Lys
XM_011535987.1:c.3137T>A	XP_011534289.1:p.Met1046Lys
XM_011535988.1:c.2000T>A	XP_011534290.1:p.Met667Lys
NM_001346813.1:c.4859T>A	NP_001333742.1:p.Met1620Lys
NM_001363725.1:c.2609T>A	NP_001350654.1:p.Met870Lys
XM_011535984.2:c.5069T>A	XP_011534286.2:p.Met1690Lys
XM_011535988.3:c.2000T>A	XP_011534290.1:p.Met667Lys
XM_017011103.2:c.4970T>A	XP_016866592.1:p.Met1657Lys
XM_017011104.1:c.4940T>A	XP_016866593.1:p.Met1647Lys
XM_017011105.2:c.4910T>A	XP_016866594.1:p.Met1637Lys
XM_017011106.2:c.4781T>A	XP_016866595.1:p.Met1594Lys
XM_017011107.2:c.4760T>A	XP_016866596.1:p.Met1587Lys
XR_002956289.1:n.5055T>A
NM_001363725.2:c.2609T>A	NP_001350654.1:p.Met870Lys
NM_001371656.1:c.4988T>A	NP_001358585.1:p.Met1663Lys
NM_001374820.1:c.4988T>A	NP_001361749.1:p.Met1663Lys
NM_001374828.1:c.5108T>A MANE Select	NP_001361757.1:p.Met1703Lys
NM_017519.3:c.4949T>A	NP_059989.3:p.Met1650Lys