Canonical Allele Identifier: CA366234139

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157189710-C-T
• MyVariant Identifiers: chr6:g.157510844C>T (hg19) ; chr6:g.157189710C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189710C>T , CM000668.2:g.157189710C>T	GRCh38
NC_000006.11:g.157510844C>T , CM000668.1:g.157510844C>T	GRCh37
NC_000006.10:g.157552536C>T	NCBI36
NG_032093.1:g.416781C>T
NG_032093.2:g.416781C>T
NG_066624.1:g.418685C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3829C>T	ENSP00000055163.8:p.Pro1277Ser
ENST00000414678.8:c.3898C>T	ENSP00000412835.3:p.Pro1300Ser
ENST00000637015.2:c.4117C>T	ENSP00000489729.2:p.Pro1373Ser
ENST00000346085.10:c.3868C>T	ENSP00000344546.5:p.Pro1290Ser
ENST00000350026.10:c.3580C>T	ENSP00000055163.7:p.Pro1194Ser
ENST00000414678.7:c.2146C>T	ENSP00000412835.2:p.Pro716Ser
ENST00000635849.1:c.1309C>T	ENSP00000490948.1:p.Pro437Ser
ENST00000635957.1:c.943C>T	ENSP00000490385.1:p.Pro315Ser
ENST00000636930.2:c.3988C>T MANE Select	ENSP00000490491.2:p.Pro1330Ser
ENST00000636940.1:n.1985C>T
ENST00000637015.1:c.1356C>T
ENST00000637568.1:c.1270C>T
ENST00000637741.1:n.654C>T
ENST00000637810.1:c.1330C>T	ENSP00000489636.1:p.Pro444Ser
ENST00000637904.1:c.1489C>T	ENSP00000490550.1:p.Pro497Ser
ENST00000647938.1:c.3619C>T	ENSP00000498155.1:p.Pro1207Ser
ENST00000346085.9:c.3619C>T	ENSP00000344546.4:p.Pro1207Ser
ENST00000350026.9:c.3580C>T	ENSP00000055163.7:p.Pro1194Ser
ENST00000414678.6:c.2146C>T	ENSP00000412835.2:p.Pro716Ser
NM_017519.2:c.3580C>T	NP_059989.2:p.Pro1194Ser
NM_020732.3:c.3619C>T	NP_065783.3:p.Pro1207Ser
XM_005267069.3:c.3739C>T	XP_005267126.2:p.Pro1247Ser
XM_011535984.1:c.2818C>T	XP_011534286.1:p.Pro940Ser
XM_011535985.1:c.2638C>T	XP_011534287.1:p.Pro880Ser
XM_011535986.1:c.2398C>T	XP_011534288.1:p.Pro800Ser
XM_011535987.1:c.2017C>T	XP_011534289.1:p.Pro673Ser
XM_011535988.1:c.880C>T	XP_011534290.1:p.Pro294Ser
NM_001346813.1:c.3739C>T	NP_001333742.1:p.Pro1247Ser
NM_001363725.1:c.1489C>T	NP_001350654.1:p.Pro497Ser
XM_011535984.2:c.3949C>T	XP_011534286.2:p.Pro1317Ser
XM_011535988.3:c.880C>T	XP_011534290.1:p.Pro294Ser
XM_017011103.2:c.3850C>T	XP_016866592.1:p.Pro1284Ser
XM_017011104.1:c.3820C>T	XP_016866593.1:p.Pro1274Ser
XM_017011105.2:c.3790C>T	XP_016866594.1:p.Pro1264Ser
XM_017011106.2:c.3661C>T	XP_016866595.1:p.Pro1221Ser
XM_017011107.2:c.3640C>T	XP_016866596.1:p.Pro1214Ser
XR_002956289.1:n.4032C>T
NM_001363725.2:c.1489C>T	NP_001350654.1:p.Pro497Ser
NM_001371656.1:c.3868C>T	NP_001358585.1:p.Pro1290Ser
NM_001374820.1:c.3868C>T	NP_001361749.1:p.Pro1290Ser
NM_001374828.1:c.3988C>T MANE Select	NP_001361757.1:p.Pro1330Ser
NM_017519.3:c.3829C>T	NP_059989.3:p.Pro1277Ser