Canonical Allele Identifier: CA366239914

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366715
• MyVariant Identifiers: chr6:g.157520039C>G (hg19) ; chr6:g.157198905C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198905C>G , CM000668.2:g.157198905C>G	GRCh38
NC_000006.11:g.157520039C>G , CM000668.1:g.157520039C>G	GRCh37
NC_000006.10:g.157561731C>G	NCBI36
NG_032093.1:g.425976C>G
NG_032093.2:g.425976C>G
NG_066624.1:g.427880C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4318C>G	ENSP00000055163.8:p.Pro1440Ala
ENST00000414678.8:c.4387C>G	ENSP00000412835.3:p.Pro1463Ala
ENST00000637015.2:c.4606C>G	ENSP00000489729.2:p.Pro1536Ala
ENST00000346085.10:c.4357C>G	ENSP00000344546.5:p.Pro1453Ala
ENST00000350026.10:c.4069C>G	ENSP00000055163.7:p.Pro1357Ala
ENST00000414678.7:c.2635C>G	ENSP00000412835.2:p.Pro879Ala
ENST00000635849.1:c.1798C>G	ENSP00000490948.1:p.Pro600Ala
ENST00000635957.1:c.1429C>G	ENSP00000490385.1:p.Pro477Ala
ENST00000636227.1:n.2940C>G
ENST00000636254.1:n.397C>G
ENST00000636930.2:c.4477C>G MANE Select	ENSP00000490491.2:p.Pro1493Ala
ENST00000636940.1:n.2474C>G
ENST00000637015.1:c.1845C>G
ENST00000637568.1:c.1759C>G
ENST00000637741.1:n.1143C>G
ENST00000637810.1:c.1819C>G	ENSP00000489636.1:p.Pro607Ala
ENST00000637904.1:c.1978C>G	ENSP00000490550.1:p.Pro660Ala
ENST00000647938.1:c.4108C>G	ENSP00000498155.1:p.Pro1370Ala
ENST00000346085.9:c.4108C>G	ENSP00000344546.4:p.Pro1370Ala
ENST00000350026.9:c.4069C>G	ENSP00000055163.7:p.Pro1357Ala
ENST00000414678.6:c.2635C>G	ENSP00000412835.2:p.Pro879Ala
NM_017519.2:c.4069C>G	NP_059989.2:p.Pro1357Ala
NM_020732.3:c.4108C>G	NP_065783.3:p.Pro1370Ala
XM_005267069.3:c.4228C>G	XP_005267126.2:p.Pro1410Ala
XM_011535984.1:c.3307C>G	XP_011534286.1:p.Pro1103Ala
XM_011535985.1:c.3127C>G	XP_011534287.1:p.Pro1043Ala
XM_011535986.1:c.2887C>G	XP_011534288.1:p.Pro963Ala
XM_011535987.1:c.2506C>G	XP_011534289.1:p.Pro836Ala
XM_011535988.1:c.1369C>G	XP_011534290.1:p.Pro457Ala
NM_001346813.1:c.4228C>G	NP_001333742.1:p.Pro1410Ala
NM_001363725.1:c.1978C>G	NP_001350654.1:p.Pro660Ala
XM_011535984.2:c.4438C>G	XP_011534286.2:p.Pro1480Ala
XM_011535988.3:c.1369C>G	XP_011534290.1:p.Pro457Ala
XM_017011103.2:c.4339C>G	XP_016866592.1:p.Pro1447Ala
XM_017011104.1:c.4309C>G	XP_016866593.1:p.Pro1437Ala
XM_017011105.2:c.4279C>G	XP_016866594.1:p.Pro1427Ala
XM_017011106.2:c.4150C>G	XP_016866595.1:p.Pro1384Ala
XM_017011107.2:c.4129C>G	XP_016866596.1:p.Pro1377Ala
XR_002956289.1:n.4427-1800C>G
NM_001363725.2:c.1978C>G	NP_001350654.1:p.Pro660Ala
NM_001371656.1:c.4357C>G	NP_001358585.1:p.Pro1453Ala
NM_001374820.1:c.4357C>G	NP_001361749.1:p.Pro1453Ala
NM_001374828.1:c.4477C>G MANE Select	NP_001361757.1:p.Pro1493Ala
NM_017519.3:c.4318C>G	NP_059989.3:p.Pro1440Ala