Canonical Allele Identifier: CA366239602

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128366082
• MyVariant Identifiers: chr6:g.157519970C>A (hg19) ; chr6:g.157198836C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198836C>A , CM000668.2:g.157198836C>A	GRCh38
NC_000006.11:g.157519970C>A , CM000668.1:g.157519970C>A	GRCh37
NC_000006.10:g.157561662C>A	NCBI36
NG_032093.1:g.425907C>A
NG_032093.2:g.425907C>A
NG_066624.1:g.427811C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4249C>A	ENSP00000055163.8:p.Pro1417Thr
ENST00000414678.8:c.4318C>A	ENSP00000412835.3:p.Pro1440Thr
ENST00000637015.2:c.4537C>A	ENSP00000489729.2:p.Pro1513Thr
ENST00000346085.10:c.4288C>A	ENSP00000344546.5:p.Pro1430Thr
ENST00000350026.10:c.4000C>A	ENSP00000055163.7:p.Pro1334Thr
ENST00000414678.7:c.2566C>A	ENSP00000412835.2:p.Pro856Thr
ENST00000635849.1:c.1729C>A	ENSP00000490948.1:p.Pro577Thr
ENST00000635957.1:c.1360C>A	ENSP00000490385.1:p.Pro454Thr
ENST00000636227.1:n.2871C>A
ENST00000636254.1:n.328C>A
ENST00000636930.2:c.4408C>A MANE Select	ENSP00000490491.2:p.Pro1470Thr
ENST00000636940.1:n.2405C>A
ENST00000637015.1:c.1776C>A
ENST00000637568.1:c.1690C>A
ENST00000637741.1:n.1074C>A
ENST00000637810.1:c.1750C>A	ENSP00000489636.1:p.Pro584Thr
ENST00000637904.1:c.1909C>A	ENSP00000490550.1:p.Pro637Thr
ENST00000647938.1:c.4039C>A	ENSP00000498155.1:p.Pro1347Thr
ENST00000346085.9:c.4039C>A	ENSP00000344546.4:p.Pro1347Thr
ENST00000350026.9:c.4000C>A	ENSP00000055163.7:p.Pro1334Thr
ENST00000414678.6:c.2566C>A	ENSP00000412835.2:p.Pro856Thr
NM_017519.2:c.4000C>A	NP_059989.2:p.Pro1334Thr
NM_020732.3:c.4039C>A	NP_065783.3:p.Pro1347Thr
XM_005267069.3:c.4159C>A	XP_005267126.2:p.Pro1387Thr
XM_011535984.1:c.3238C>A	XP_011534286.1:p.Pro1080Thr
XM_011535985.1:c.3058C>A	XP_011534287.1:p.Pro1020Thr
XM_011535986.1:c.2818C>A	XP_011534288.1:p.Pro940Thr
XM_011535987.1:c.2437C>A	XP_011534289.1:p.Pro813Thr
XM_011535988.1:c.1300C>A	XP_011534290.1:p.Pro434Thr
NM_001346813.1:c.4159C>A	NP_001333742.1:p.Pro1387Thr
NM_001363725.1:c.1909C>A	NP_001350654.1:p.Pro637Thr
XM_011535984.2:c.4369C>A	XP_011534286.2:p.Pro1457Thr
XM_011535988.3:c.1300C>A	XP_011534290.1:p.Pro434Thr
XM_017011103.2:c.4270C>A	XP_016866592.1:p.Pro1424Thr
XM_017011104.1:c.4240C>A	XP_016866593.1:p.Pro1414Thr
XM_017011105.2:c.4210C>A	XP_016866594.1:p.Pro1404Thr
XM_017011106.2:c.4081C>A	XP_016866595.1:p.Pro1361Thr
XM_017011107.2:c.4060C>A	XP_016866596.1:p.Pro1354Thr
XR_002956289.1:n.4427-1869C>A
NM_001363725.2:c.1909C>A	NP_001350654.1:p.Pro637Thr
NM_001371656.1:c.4288C>A	NP_001358585.1:p.Pro1430Thr
NM_001374820.1:c.4288C>A	NP_001361749.1:p.Pro1430Thr
NM_001374828.1:c.4408C>A MANE Select	NP_001361757.1:p.Pro1470Thr
NM_017519.3:c.4249C>A	NP_059989.3:p.Pro1417Thr