Canonical Allele Identifier: CA366239611

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157519971C>A (hg19) ; chr6:g.157198837C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157198837C>A , CM000668.2:g.157198837C>A	GRCh38
NC_000006.11:g.157519971C>A , CM000668.1:g.157519971C>A	GRCh37
NC_000006.10:g.157561663C>A	NCBI36
NG_032093.1:g.425908C>A
NG_032093.2:g.425908C>A
NG_066624.1:g.427812C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4250C>A	ENSP00000055163.8:p.Pro1417Gln
ENST00000414678.8:c.4319C>A	ENSP00000412835.3:p.Pro1440Gln
ENST00000637015.2:c.4538C>A	ENSP00000489729.2:p.Pro1513Gln
ENST00000346085.10:c.4289C>A	ENSP00000344546.5:p.Pro1430Gln
ENST00000350026.10:c.4001C>A	ENSP00000055163.7:p.Pro1334Gln
ENST00000414678.7:c.2567C>A	ENSP00000412835.2:p.Pro856Gln
ENST00000635849.1:c.1730C>A	ENSP00000490948.1:p.Pro577Gln
ENST00000635957.1:c.1361C>A	ENSP00000490385.1:p.Pro454Gln
ENST00000636227.1:n.2872C>A
ENST00000636254.1:n.329C>A
ENST00000636930.2:c.4409C>A MANE Select	ENSP00000490491.2:p.Pro1470Gln
ENST00000636940.1:n.2406C>A
ENST00000637015.1:c.1777C>A
ENST00000637568.1:c.1691C>A
ENST00000637741.1:n.1075C>A
ENST00000637810.1:c.1751C>A	ENSP00000489636.1:p.Pro584Gln
ENST00000637904.1:c.1910C>A	ENSP00000490550.1:p.Pro637Gln
ENST00000647938.1:c.4040C>A	ENSP00000498155.1:p.Pro1347Gln
ENST00000346085.9:c.4040C>A	ENSP00000344546.4:p.Pro1347Gln
ENST00000350026.9:c.4001C>A	ENSP00000055163.7:p.Pro1334Gln
ENST00000414678.6:c.2567C>A	ENSP00000412835.2:p.Pro856Gln
NM_017519.2:c.4001C>A	NP_059989.2:p.Pro1334Gln
NM_020732.3:c.4040C>A	NP_065783.3:p.Pro1347Gln
XM_005267069.3:c.4160C>A	XP_005267126.2:p.Pro1387Gln
XM_011535984.1:c.3239C>A	XP_011534286.1:p.Pro1080Gln
XM_011535985.1:c.3059C>A	XP_011534287.1:p.Pro1020Gln
XM_011535986.1:c.2819C>A	XP_011534288.1:p.Pro940Gln
XM_011535987.1:c.2438C>A	XP_011534289.1:p.Pro813Gln
XM_011535988.1:c.1301C>A	XP_011534290.1:p.Pro434Gln
NM_001346813.1:c.4160C>A	NP_001333742.1:p.Pro1387Gln
NM_001363725.1:c.1910C>A	NP_001350654.1:p.Pro637Gln
XM_011535984.2:c.4370C>A	XP_011534286.2:p.Pro1457Gln
XM_011535988.3:c.1301C>A	XP_011534290.1:p.Pro434Gln
XM_017011103.2:c.4271C>A	XP_016866592.1:p.Pro1424Gln
XM_017011104.1:c.4241C>A	XP_016866593.1:p.Pro1414Gln
XM_017011105.2:c.4211C>A	XP_016866594.1:p.Pro1404Gln
XM_017011106.2:c.4082C>A	XP_016866595.1:p.Pro1361Gln
XM_017011107.2:c.4061C>A	XP_016866596.1:p.Pro1354Gln
XR_002956289.1:n.4427-1868C>A
NM_001363725.2:c.1910C>A	NP_001350654.1:p.Pro637Gln
NM_001371656.1:c.4289C>A	NP_001358585.1:p.Pro1430Gln
NM_001374820.1:c.4289C>A	NP_001361749.1:p.Pro1430Gln
NM_001374828.1:c.4409C>A MANE Select	NP_001361757.1:p.Pro1470Gln
NM_017519.3:c.4250C>A	NP_059989.3:p.Pro1417Gln