Canonical Allele Identifier: CA366242337

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522386C>G (hg19) ; chr6:g.157201252C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201252C>G , CM000668.2:g.157201252C>G	GRCh38
NC_000006.11:g.157522386C>G , CM000668.1:g.157522386C>G	GRCh37
NC_000006.10:g.157564078C>G	NCBI36
NG_032093.1:g.428323C>G
NG_032093.2:g.428323C>G
NG_066624.1:g.430227C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4868C>G	ENSP00000055163.8:p.Ala1623Gly
ENST00000414678.8:c.4937C>G	ENSP00000412835.3:p.Ala1646Gly
ENST00000637015.2:c.5156C>G	ENSP00000489729.2:p.Ala1719Gly
ENST00000346085.10:c.4907C>G	ENSP00000344546.5:p.Ala1636Gly
ENST00000350026.10:c.4619C>G	ENSP00000055163.7:p.Ala1540Gly
ENST00000414678.7:c.3185C>G	ENSP00000412835.2:p.Ala1062Gly
ENST00000635849.1:c.2348C>G	ENSP00000490948.1:p.Ala783Gly
ENST00000635957.1:c.1979C>G	ENSP00000490385.1:p.Ala660Gly
ENST00000636227.1:n.3490C>G
ENST00000636254.1:n.947C>G
ENST00000636930.2:c.5027C>G MANE Select	ENSP00000490491.2:p.Ala1676Gly
ENST00000636940.1:n.3024C>G
ENST00000637015.1:c.2395C>G
ENST00000637568.1:c.2309C>G
ENST00000637741.1:n.1693C>G
ENST00000637810.1:c.2369C>G	ENSP00000489636.1:p.Ala790Gly
ENST00000637904.1:c.2528C>G	ENSP00000490550.1:p.Ala843Gly
ENST00000647938.1:c.4658C>G	ENSP00000498155.1:p.Ala1553Gly
ENST00000346085.9:c.4658C>G	ENSP00000344546.4:p.Ala1553Gly
ENST00000350026.9:c.4619C>G	ENSP00000055163.7:p.Ala1540Gly
ENST00000414678.6:c.3185C>G	ENSP00000412835.2:p.Ala1062Gly
NM_017519.2:c.4619C>G	NP_059989.2:p.Ala1540Gly
NM_020732.3:c.4658C>G	NP_065783.3:p.Ala1553Gly
XM_005267069.3:c.4778C>G	XP_005267126.2:p.Ala1593Gly
XM_011535984.1:c.3857C>G	XP_011534286.1:p.Ala1286Gly
XM_011535985.1:c.3677C>G	XP_011534287.1:p.Ala1226Gly
XM_011535986.1:c.3437C>G	XP_011534288.1:p.Ala1146Gly
XM_011535987.1:c.3056C>G	XP_011534289.1:p.Ala1019Gly
XM_011535988.1:c.1919C>G	XP_011534290.1:p.Ala640Gly
NM_001346813.1:c.4778C>G	NP_001333742.1:p.Ala1593Gly
NM_001363725.1:c.2528C>G	NP_001350654.1:p.Ala843Gly
XM_011535984.2:c.4988C>G	XP_011534286.2:p.Ala1663Gly
XM_011535988.3:c.1919C>G	XP_011534290.1:p.Ala640Gly
XM_017011103.2:c.4889C>G	XP_016866592.1:p.Ala1630Gly
XM_017011104.1:c.4859C>G	XP_016866593.1:p.Ala1620Gly
XM_017011105.2:c.4829C>G	XP_016866594.1:p.Ala1610Gly
XM_017011106.2:c.4700C>G	XP_016866595.1:p.Ala1567Gly
XM_017011107.2:c.4679C>G	XP_016866596.1:p.Ala1560Gly
XR_002956289.1:n.4974C>G
NM_001363725.2:c.2528C>G	NP_001350654.1:p.Ala843Gly
NM_001371656.1:c.4907C>G	NP_001358585.1:p.Ala1636Gly
NM_001374820.1:c.4907C>G	NP_001361749.1:p.Ala1636Gly
NM_001374828.1:c.5027C>G MANE Select	NP_001361757.1:p.Ala1676Gly
NM_017519.3:c.4868C>G	NP_059989.3:p.Ala1623Gly