Canonical Allele Identifier: CA366227532

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317028
• gnomAD v4: 6-157181045-T-C
• MyVariant Identifiers: chr6:g.157502179T>C (hg19) ; chr6:g.157181045T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181045T>C , CM000668.2:g.157181045T>C	GRCh38
NC_000006.11:g.157502179T>C , CM000668.1:g.157502179T>C	GRCh37
NC_000006.10:g.157543871T>C	NCBI36
NG_032093.1:g.408116T>C
NG_032093.2:g.408116T>C
NG_066624.1:g.410020T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3422T>C	ENSP00000055163.8:p.Leu1141Pro
ENST00000414678.8:c.3491T>C	ENSP00000412835.3:p.Leu1164Pro
ENST00000637015.2:c.3710T>C	ENSP00000489729.2:p.Leu1237Pro
ENST00000319584.11:c.1595T>C	ENSP00000313006.7:p.Leu532Pro
ENST00000346085.10:c.3461T>C	ENSP00000344546.5:p.Leu1154Pro
ENST00000350026.10:c.3173T>C	ENSP00000055163.7:p.Leu1058Pro
ENST00000414678.7:c.1739T>C	ENSP00000412835.2:p.Leu580Pro
ENST00000635849.1:c.902T>C	ENSP00000490948.1:p.Leu301Pro
ENST00000635957.1:c.536T>C	ENSP00000490385.1:p.Leu179Pro
ENST00000636930.2:c.3581T>C MANE Select	ENSP00000490491.2:p.Leu1194Pro
ENST00000636940.1:n.1578T>C
ENST00000637015.1:c.949T>C
ENST00000637568.1:c.863T>C
ENST00000637741.1:n.247T>C
ENST00000637810.1:c.923T>C	ENSP00000489636.1:p.Leu308Pro
ENST00000637904.1:c.1082T>C	ENSP00000490550.1:p.Leu361Pro
ENST00000647938.1:c.3212T>C	ENSP00000498155.1:p.Leu1071Pro
ENST00000319584.10:c.1598T>C	ENSP00000313006.6:p.Leu533Pro
ENST00000346085.9:c.3212T>C	ENSP00000344546.4:p.Leu1071Pro
ENST00000350026.9:c.3173T>C	ENSP00000055163.7:p.Leu1058Pro
ENST00000400790.3:c.374T>C	ENSP00000383596.3:p.Leu125Pro
ENST00000414678.6:c.1739T>C	ENSP00000412835.2:p.Leu580Pro
ENST00000478761.3:c.783T>C
NM_017519.2:c.3173T>C	NP_059989.2:p.Leu1058Pro
NM_020732.3:c.3212T>C	NP_065783.3:p.Leu1071Pro
XM_005267069.3:c.3332T>C	XP_005267126.2:p.Leu1111Pro
XM_011535984.1:c.2411T>C	XP_011534286.1:p.Leu804Pro
XM_011535985.1:c.2231T>C	XP_011534287.1:p.Leu744Pro
XM_011535986.1:c.1991T>C	XP_011534288.1:p.Leu664Pro
XM_011535987.1:c.1610T>C	XP_011534289.1:p.Leu537Pro
XM_011535988.1:c.473T>C	XP_011534290.1:p.Leu158Pro
NM_001346813.1:c.3332T>C	NP_001333742.1:p.Leu1111Pro
NM_001363725.1:c.1082T>C	NP_001350654.1:p.Leu361Pro
XM_011535984.2:c.3542T>C	XP_011534286.2:p.Leu1181Pro
XM_011535988.3:c.473T>C	XP_011534290.1:p.Leu158Pro
XM_017011103.2:c.3443T>C	XP_016866592.1:p.Leu1148Pro
XM_017011104.1:c.3413T>C	XP_016866593.1:p.Leu1138Pro
XM_017011105.2:c.3383T>C	XP_016866594.1:p.Leu1128Pro
XM_017011106.2:c.3254T>C	XP_016866595.1:p.Leu1085Pro
XM_017011107.2:c.3233T>C	XP_016866596.1:p.Leu1078Pro
XR_002956289.1:n.3625T>C
NM_001363725.2:c.1082T>C	NP_001350654.1:p.Leu361Pro
NM_001371656.1:c.3461T>C	NP_001358585.1:p.Leu1154Pro
NM_001374820.1:c.3461T>C	NP_001361749.1:p.Leu1154Pro
NM_001374828.1:c.3581T>C MANE Select	NP_001361757.1:p.Leu1194Pro
NM_017519.3:c.3422T>C	NP_059989.3:p.Leu1141Pro