Canonical Allele Identifier: CA366242074

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201131-C-T
• MyVariant Identifiers: chr6:g.157522265C>T (hg19) ; chr6:g.157201131C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201131C>T , CM000668.2:g.157201131C>T	GRCh38
NC_000006.11:g.157522265C>T , CM000668.1:g.157522265C>T	GRCh37
NC_000006.10:g.157563957C>T	NCBI36
NG_032093.1:g.428202C>T
NG_032093.2:g.428202C>T
NG_066624.1:g.430106C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4747C>T	ENSP00000055163.8:p.Pro1583Ser
ENST00000414678.8:c.4816C>T	ENSP00000412835.3:p.Pro1606Ser
ENST00000637015.2:c.5035C>T	ENSP00000489729.2:p.Pro1679Ser
ENST00000346085.10:c.4786C>T	ENSP00000344546.5:p.Pro1596Ser
ENST00000350026.10:c.4498C>T	ENSP00000055163.7:p.Pro1500Ser
ENST00000414678.7:c.3064C>T	ENSP00000412835.2:p.Pro1022Ser
ENST00000635849.1:c.2227C>T	ENSP00000490948.1:p.Pro743Ser
ENST00000635957.1:c.1858C>T	ENSP00000490385.1:p.Pro620Ser
ENST00000636227.1:n.3369C>T
ENST00000636254.1:n.826C>T
ENST00000636930.2:c.4906C>T MANE Select	ENSP00000490491.2:p.Pro1636Ser
ENST00000636940.1:n.2903C>T
ENST00000637015.1:c.2274C>T
ENST00000637568.1:c.2188C>T
ENST00000637741.1:n.1572C>T
ENST00000637810.1:c.2248C>T	ENSP00000489636.1:p.Pro750Ser
ENST00000637904.1:c.2407C>T	ENSP00000490550.1:p.Pro803Ser
ENST00000647938.1:c.4537C>T	ENSP00000498155.1:p.Pro1513Ser
ENST00000346085.9:c.4537C>T	ENSP00000344546.4:p.Pro1513Ser
ENST00000350026.9:c.4498C>T	ENSP00000055163.7:p.Pro1500Ser
ENST00000414678.6:c.3064C>T	ENSP00000412835.2:p.Pro1022Ser
NM_017519.2:c.4498C>T	NP_059989.2:p.Pro1500Ser
NM_020732.3:c.4537C>T	NP_065783.3:p.Pro1513Ser
XM_005267069.3:c.4657C>T	XP_005267126.2:p.Pro1553Ser
XM_011535984.1:c.3736C>T	XP_011534286.1:p.Pro1246Ser
XM_011535985.1:c.3556C>T	XP_011534287.1:p.Pro1186Ser
XM_011535986.1:c.3316C>T	XP_011534288.1:p.Pro1106Ser
XM_011535987.1:c.2935C>T	XP_011534289.1:p.Pro979Ser
XM_011535988.1:c.1798C>T	XP_011534290.1:p.Pro600Ser
NM_001346813.1:c.4657C>T	NP_001333742.1:p.Pro1553Ser
NM_001363725.1:c.2407C>T	NP_001350654.1:p.Pro803Ser
XM_011535984.2:c.4867C>T	XP_011534286.2:p.Pro1623Ser
XM_011535988.3:c.1798C>T	XP_011534290.1:p.Pro600Ser
XM_017011103.2:c.4768C>T	XP_016866592.1:p.Pro1590Ser
XM_017011104.1:c.4738C>T	XP_016866593.1:p.Pro1580Ser
XM_017011105.2:c.4708C>T	XP_016866594.1:p.Pro1570Ser
XM_017011106.2:c.4579C>T	XP_016866595.1:p.Pro1527Ser
XM_017011107.2:c.4558C>T	XP_016866596.1:p.Pro1520Ser
XR_002956289.1:n.4853C>T
NM_001363725.2:c.2407C>T	NP_001350654.1:p.Pro803Ser
NM_001371656.1:c.4786C>T	NP_001358585.1:p.Pro1596Ser
NM_001374820.1:c.4786C>T	NP_001361749.1:p.Pro1596Ser
NM_001374828.1:c.4906C>T MANE Select	NP_001361757.1:p.Pro1636Ser
NM_017519.3:c.4747C>T	NP_059989.3:p.Pro1583Ser