Canonical Allele Identifier: CA366234290

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510896C>G (hg19) ; chr6:g.157189762C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189762C>G , CM000668.2:g.157189762C>G	GRCh38
NC_000006.11:g.157510896C>G , CM000668.1:g.157510896C>G	GRCh37
NC_000006.10:g.157552588C>G	NCBI36
NG_032093.1:g.416833C>G
NG_032093.2:g.416833C>G
NG_066624.1:g.418737C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3881C>G	ENSP00000055163.8:p.Thr1294Ser
ENST00000414678.8:c.3950C>G	ENSP00000412835.3:p.Thr1317Ser
ENST00000637015.2:c.4169C>G	ENSP00000489729.2:p.Thr1390Ser
ENST00000346085.10:c.3920C>G	ENSP00000344546.5:p.Thr1307Ser
ENST00000350026.10:c.3632C>G	ENSP00000055163.7:p.Thr1211Ser
ENST00000414678.7:c.2198C>G	ENSP00000412835.2:p.Thr733Ser
ENST00000635849.1:c.1361C>G	ENSP00000490948.1:p.Thr454Ser
ENST00000635957.1:c.995C>G	ENSP00000490385.1:p.Thr332Ser
ENST00000636930.2:c.4040C>G MANE Select	ENSP00000490491.2:p.Thr1347Ser
ENST00000636940.1:n.2037C>G
ENST00000637015.1:c.1408C>G
ENST00000637568.1:c.1322C>G
ENST00000637741.1:n.706C>G
ENST00000637810.1:c.1382C>G	ENSP00000489636.1:p.Thr461Ser
ENST00000637904.1:c.1541C>G	ENSP00000490550.1:p.Thr514Ser
ENST00000647938.1:c.3671C>G	ENSP00000498155.1:p.Thr1224Ser
ENST00000346085.9:c.3671C>G	ENSP00000344546.4:p.Thr1224Ser
ENST00000350026.9:c.3632C>G	ENSP00000055163.7:p.Thr1211Ser
ENST00000414678.6:c.2198C>G	ENSP00000412835.2:p.Thr733Ser
NM_017519.2:c.3632C>G	NP_059989.2:p.Thr1211Ser
NM_020732.3:c.3671C>G	NP_065783.3:p.Thr1224Ser
XM_005267069.3:c.3791C>G	XP_005267126.2:p.Thr1264Ser
XM_011535984.1:c.2870C>G	XP_011534286.1:p.Thr957Ser
XM_011535985.1:c.2690C>G	XP_011534287.1:p.Thr897Ser
XM_011535986.1:c.2450C>G	XP_011534288.1:p.Thr817Ser
XM_011535987.1:c.2069C>G	XP_011534289.1:p.Thr690Ser
XM_011535988.1:c.932C>G	XP_011534290.1:p.Thr311Ser
NM_001346813.1:c.3791C>G	NP_001333742.1:p.Thr1264Ser
NM_001363725.1:c.1541C>G	NP_001350654.1:p.Thr514Ser
XM_011535984.2:c.4001C>G	XP_011534286.2:p.Thr1334Ser
XM_011535988.3:c.932C>G	XP_011534290.1:p.Thr311Ser
XM_017011103.2:c.3902C>G	XP_016866592.1:p.Thr1301Ser
XM_017011104.1:c.3872C>G	XP_016866593.1:p.Thr1291Ser
XM_017011105.2:c.3842C>G	XP_016866594.1:p.Thr1281Ser
XM_017011106.2:c.3713C>G	XP_016866595.1:p.Thr1238Ser
XM_017011107.2:c.3692C>G	XP_016866596.1:p.Thr1231Ser
XR_002956289.1:n.4084C>G
NM_001363725.2:c.1541C>G	NP_001350654.1:p.Thr514Ser
NM_001371656.1:c.3920C>G	NP_001358585.1:p.Thr1307Ser
NM_001374820.1:c.3920C>G	NP_001361749.1:p.Thr1307Ser
NM_001374828.1:c.4040C>G MANE Select	NP_001361757.1:p.Thr1347Ser
NM_017519.3:c.3881C>G	NP_059989.3:p.Thr1294Ser