Canonical Allele Identifier: CA366242607

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 450039
• ClinVar RCV Id: RCV000521189
• dbSNP Id: rs1554235950
• COSMIC: COSM3859987 ; COSM3859988
• MyVariant Identifiers: chr6:g.157522469C>T (hg19) ; chr6:g.157201335C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201335C>T , CM000668.2:g.157201335C>T	GRCh38
NC_000006.11:g.157522469C>T , CM000668.1:g.157522469C>T	GRCh37
NC_000006.10:g.157564161C>T	NCBI36
NG_032093.1:g.428406C>T
NG_032093.2:g.428406C>T
NG_066624.1:g.430310C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4951C>T	ENSP00000055163.8:p.Gln1651Ter
ENST00000414678.8:c.5020C>T	ENSP00000412835.3:p.Gln1674Ter
ENST00000637015.2:c.5239C>T	ENSP00000489729.2:p.Gln1747Ter
ENST00000346085.10:c.4990C>T	ENSP00000344546.5:p.Gln1664Ter
ENST00000350026.10:c.4702C>T	ENSP00000055163.7:p.Gln1568Ter
ENST00000414678.7:c.3268C>T	ENSP00000412835.2:p.Gln1090Ter
ENST00000635849.1:c.2431C>T	ENSP00000490948.1:p.Gln811Ter
ENST00000635957.1:c.2062C>T	ENSP00000490385.1:p.Gln688Ter
ENST00000636227.1:n.3573C>T
ENST00000636254.1:n.1030C>T
ENST00000636930.2:c.5110C>T MANE Select	ENSP00000490491.2:p.Gln1704Ter
ENST00000636940.1:n.3107C>T
ENST00000637015.1:c.2478C>T
ENST00000637568.1:c.2392C>T
ENST00000637741.1:n.1776C>T
ENST00000637810.1:c.2452C>T	ENSP00000489636.1:p.Gln818Ter
ENST00000637904.1:c.2611C>T	ENSP00000490550.1:p.Gln871Ter
ENST00000647938.1:c.4741C>T	ENSP00000498155.1:p.Gln1581Ter
ENST00000346085.9:c.4741C>T	ENSP00000344546.4:p.Gln1581Ter
ENST00000350026.9:c.4702C>T	ENSP00000055163.7:p.Gln1568Ter
ENST00000414678.6:c.3268C>T	ENSP00000412835.2:p.Gln1090Ter
NM_017519.2:c.4702C>T	NP_059989.2:p.Gln1568Ter
NM_020732.3:c.4741C>T	NP_065783.3:p.Gln1581Ter
XM_005267069.3:c.4861C>T	XP_005267126.2:p.Gln1621Ter
XM_011535984.1:c.3940C>T	XP_011534286.1:p.Gln1314Ter
XM_011535985.1:c.3760C>T	XP_011534287.1:p.Gln1254Ter
XM_011535986.1:c.3520C>T	XP_011534288.1:p.Gln1174Ter
XM_011535987.1:c.3139C>T	XP_011534289.1:p.Gln1047Ter
XM_011535988.1:c.2002C>T	XP_011534290.1:p.Gln668Ter
NM_001346813.1:c.4861C>T	NP_001333742.1:p.Gln1621Ter
NM_001363725.1:c.2611C>T	NP_001350654.1:p.Gln871Ter
XM_011535984.2:c.5071C>T	XP_011534286.2:p.Gln1691Ter
XM_011535988.3:c.2002C>T	XP_011534290.1:p.Gln668Ter
XM_017011103.2:c.4972C>T	XP_016866592.1:p.Gln1658Ter
XM_017011104.1:c.4942C>T	XP_016866593.1:p.Gln1648Ter
XM_017011105.2:c.4912C>T	XP_016866594.1:p.Gln1638Ter
XM_017011106.2:c.4783C>T	XP_016866595.1:p.Gln1595Ter
XM_017011107.2:c.4762C>T	XP_016866596.1:p.Gln1588Ter
XR_002956289.1:n.5057C>T
NM_001363725.2:c.2611C>T	NP_001350654.1:p.Gln871Ter
NM_001371656.1:c.4990C>T	NP_001358585.1:p.Gln1664Ter
NM_001374820.1:c.4990C>T	NP_001361749.1:p.Gln1664Ter
NM_001374828.1:c.5110C>T MANE Select	NP_001361757.1:p.Gln1704Ter
NM_017519.3:c.4951C>T	NP_059989.3:p.Gln1651Ter