Canonical Allele Identifier: CA366239916

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366715
• gnomAD v4: 6-157198905-C-T
• MyVariant Identifiers: chr6:g.157520039C>T (hg19) ; chr6:g.157198905C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4318C>T	ENSP00000055163.8:p.Pro1440Ser
ENST00000414678.8:c.4387C>T	ENSP00000412835.3:p.Pro1463Ser
ENST00000637015.2:c.4606C>T	ENSP00000489729.2:p.Pro1536Ser
ENST00000346085.10:c.4357C>T	ENSP00000344546.5:p.Pro1453Ser
ENST00000350026.10:c.4069C>T	ENSP00000055163.7:p.Pro1357Ser
ENST00000414678.7:c.2635C>T	ENSP00000412835.2:p.Pro879Ser
ENST00000635849.1:c.1798C>T	ENSP00000490948.1:p.Pro600Ser
ENST00000635957.1:c.1429C>T	ENSP00000490385.1:p.Pro477Ser
ENST00000636227.1:n.2940C>T
ENST00000636254.1:n.397C>T
ENST00000636930.2:c.4477C>T MANE Select	ENSP00000490491.2:p.Pro1493Ser
ENST00000636940.1:n.2474C>T
ENST00000637015.1:c.1845C>T
ENST00000637568.1:c.1759C>T
ENST00000637741.1:n.1143C>T
ENST00000637810.1:c.1819C>T	ENSP00000489636.1:p.Pro607Ser
ENST00000637904.1:c.1978C>T	ENSP00000490550.1:p.Pro660Ser
ENST00000647938.1:c.4108C>T	ENSP00000498155.1:p.Pro1370Ser
ENST00000346085.9:c.4108C>T	ENSP00000344546.4:p.Pro1370Ser
ENST00000350026.9:c.4069C>T	ENSP00000055163.7:p.Pro1357Ser
ENST00000414678.6:c.2635C>T	ENSP00000412835.2:p.Pro879Ser
NM_017519.2:c.4069C>T	NP_059989.2:p.Pro1357Ser
NM_020732.3:c.4108C>T	NP_065783.3:p.Pro1370Ser
XM_005267069.3:c.4228C>T	XP_005267126.2:p.Pro1410Ser
XM_011535984.1:c.3307C>T	XP_011534286.1:p.Pro1103Ser
XM_011535985.1:c.3127C>T	XP_011534287.1:p.Pro1043Ser
XM_011535986.1:c.2887C>T	XP_011534288.1:p.Pro963Ser
XM_011535987.1:c.2506C>T	XP_011534289.1:p.Pro836Ser
XM_011535988.1:c.1369C>T	XP_011534290.1:p.Pro457Ser
NM_001346813.1:c.4228C>T	NP_001333742.1:p.Pro1410Ser
NM_001363725.1:c.1978C>T	NP_001350654.1:p.Pro660Ser
XM_011535984.2:c.4438C>T	XP_011534286.2:p.Pro1480Ser
XM_011535988.3:c.1369C>T	XP_011534290.1:p.Pro457Ser
XM_017011103.2:c.4339C>T	XP_016866592.1:p.Pro1447Ser
XM_017011104.1:c.4309C>T	XP_016866593.1:p.Pro1437Ser
XM_017011105.2:c.4279C>T	XP_016866594.1:p.Pro1427Ser
XM_017011106.2:c.4150C>T	XP_016866595.1:p.Pro1384Ser
XM_017011107.2:c.4129C>T	XP_016866596.1:p.Pro1377Ser
XR_002956289.1:n.4427-1800C>T
NM_001363725.2:c.1978C>T	NP_001350654.1:p.Pro660Ser
NM_001371656.1:c.4357C>T	NP_001358585.1:p.Pro1453Ser
NM_001374820.1:c.4357C>T	NP_001361749.1:p.Pro1453Ser
NM_001374828.1:c.4477C>T MANE Select	NP_001361757.1:p.Pro1493Ser
NM_017519.3:c.4318C>T	NP_059989.3:p.Pro1440Ser