Canonical Allele Identifier: CA366227514

Gene: ARID1B

Linked Data

• dbSNP Id: rs1232184565
• MyVariant Identifiers: chr6:g.157502178C>A (hg19) ; chr6:g.157181044C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181044C>A , CM000668.2:g.157181044C>A	GRCh38
NC_000006.11:g.157502178C>A , CM000668.1:g.157502178C>A	GRCh37
NC_000006.10:g.157543870C>A	NCBI36
NG_032093.1:g.408115C>A
NG_032093.2:g.408115C>A
NG_066624.1:g.410019C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3421C>A	ENSP00000055163.8:p.Leu1141Ile
ENST00000414678.8:c.3490C>A	ENSP00000412835.3:p.Leu1164Ile
ENST00000637015.2:c.3709C>A	ENSP00000489729.2:p.Leu1237Ile
ENST00000319584.11:c.1594C>A	ENSP00000313006.7:p.Leu532Ile
ENST00000346085.10:c.3460C>A	ENSP00000344546.5:p.Leu1154Ile
ENST00000350026.10:c.3172C>A	ENSP00000055163.7:p.Leu1058Ile
ENST00000414678.7:c.1738C>A	ENSP00000412835.2:p.Leu580Ile
ENST00000635849.1:c.901C>A	ENSP00000490948.1:p.Leu301Ile
ENST00000635957.1:c.535C>A	ENSP00000490385.1:p.Leu179Ile
ENST00000636930.2:c.3580C>A MANE Select	ENSP00000490491.2:p.Leu1194Ile
ENST00000636940.1:n.1577C>A
ENST00000637015.1:c.948C>A
ENST00000637568.1:c.862C>A
ENST00000637741.1:n.246C>A
ENST00000637810.1:c.922C>A	ENSP00000489636.1:p.Leu308Ile
ENST00000637904.1:c.1081C>A	ENSP00000490550.1:p.Leu361Ile
ENST00000647938.1:c.3211C>A	ENSP00000498155.1:p.Leu1071Ile
ENST00000319584.10:c.1597C>A	ENSP00000313006.6:p.Leu533Ile
ENST00000346085.9:c.3211C>A	ENSP00000344546.4:p.Leu1071Ile
ENST00000350026.9:c.3172C>A	ENSP00000055163.7:p.Leu1058Ile
ENST00000400790.3:c.373C>A	ENSP00000383596.3:p.Leu125Ile
ENST00000414678.6:c.1738C>A	ENSP00000412835.2:p.Leu580Ile
ENST00000478761.3:c.782C>A
NM_017519.2:c.3172C>A	NP_059989.2:p.Leu1058Ile
NM_020732.3:c.3211C>A	NP_065783.3:p.Leu1071Ile
XM_005267069.3:c.3331C>A	XP_005267126.2:p.Leu1111Ile
XM_011535984.1:c.2410C>A	XP_011534286.1:p.Leu804Ile
XM_011535985.1:c.2230C>A	XP_011534287.1:p.Leu744Ile
XM_011535986.1:c.1990C>A	XP_011534288.1:p.Leu664Ile
XM_011535987.1:c.1609C>A	XP_011534289.1:p.Leu537Ile
XM_011535988.1:c.472C>A	XP_011534290.1:p.Leu158Ile
NM_001346813.1:c.3331C>A	NP_001333742.1:p.Leu1111Ile
NM_001363725.1:c.1081C>A	NP_001350654.1:p.Leu361Ile
XM_011535984.2:c.3541C>A	XP_011534286.2:p.Leu1181Ile
XM_011535988.3:c.472C>A	XP_011534290.1:p.Leu158Ile
XM_017011103.2:c.3442C>A	XP_016866592.1:p.Leu1148Ile
XM_017011104.1:c.3412C>A	XP_016866593.1:p.Leu1138Ile
XM_017011105.2:c.3382C>A	XP_016866594.1:p.Leu1128Ile
XM_017011106.2:c.3253C>A	XP_016866595.1:p.Leu1085Ile
XM_017011107.2:c.3232C>A	XP_016866596.1:p.Leu1078Ile
XR_002956289.1:n.3624C>A
NM_001363725.2:c.1081C>A	NP_001350654.1:p.Leu361Ile
NM_001371656.1:c.3460C>A	NP_001358585.1:p.Leu1154Ile
NM_001374820.1:c.3460C>A	NP_001361749.1:p.Leu1154Ile
NM_001374828.1:c.3580C>A MANE Select	NP_001361757.1:p.Leu1194Ile
NM_017519.3:c.3421C>A	NP_059989.3:p.Leu1141Ile