Canonical Allele Identifier: CA366242605

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522469C>G (hg19) ; chr6:g.157201335C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4951C>G	ENSP00000055163.8:p.Gln1651Glu
ENST00000414678.8:c.5020C>G	ENSP00000412835.3:p.Gln1674Glu
ENST00000637015.2:c.5239C>G	ENSP00000489729.2:p.Gln1747Glu
ENST00000346085.10:c.4990C>G	ENSP00000344546.5:p.Gln1664Glu
ENST00000350026.10:c.4702C>G	ENSP00000055163.7:p.Gln1568Glu
ENST00000414678.7:c.3268C>G	ENSP00000412835.2:p.Gln1090Glu
ENST00000635849.1:c.2431C>G	ENSP00000490948.1:p.Gln811Glu
ENST00000635957.1:c.2062C>G	ENSP00000490385.1:p.Gln688Glu
ENST00000636227.1:n.3573C>G
ENST00000636254.1:n.1030C>G
ENST00000636930.2:c.5110C>G MANE Select	ENSP00000490491.2:p.Gln1704Glu
ENST00000636940.1:n.3107C>G
ENST00000637015.1:c.2478C>G
ENST00000637568.1:c.2392C>G
ENST00000637741.1:n.1776C>G
ENST00000637810.1:c.2452C>G	ENSP00000489636.1:p.Gln818Glu
ENST00000637904.1:c.2611C>G	ENSP00000490550.1:p.Gln871Glu
ENST00000647938.1:c.4741C>G	ENSP00000498155.1:p.Gln1581Glu
ENST00000346085.9:c.4741C>G	ENSP00000344546.4:p.Gln1581Glu
ENST00000350026.9:c.4702C>G	ENSP00000055163.7:p.Gln1568Glu
ENST00000414678.6:c.3268C>G	ENSP00000412835.2:p.Gln1090Glu
NM_017519.2:c.4702C>G	NP_059989.2:p.Gln1568Glu
NM_020732.3:c.4741C>G	NP_065783.3:p.Gln1581Glu
XM_005267069.3:c.4861C>G	XP_005267126.2:p.Gln1621Glu
XM_011535984.1:c.3940C>G	XP_011534286.1:p.Gln1314Glu
XM_011535985.1:c.3760C>G	XP_011534287.1:p.Gln1254Glu
XM_011535986.1:c.3520C>G	XP_011534288.1:p.Gln1174Glu
XM_011535987.1:c.3139C>G	XP_011534289.1:p.Gln1047Glu
XM_011535988.1:c.2002C>G	XP_011534290.1:p.Gln668Glu
NM_001346813.1:c.4861C>G	NP_001333742.1:p.Gln1621Glu
NM_001363725.1:c.2611C>G	NP_001350654.1:p.Gln871Glu
XM_011535984.2:c.5071C>G	XP_011534286.2:p.Gln1691Glu
XM_011535988.3:c.2002C>G	XP_011534290.1:p.Gln668Glu
XM_017011103.2:c.4972C>G	XP_016866592.1:p.Gln1658Glu
XM_017011104.1:c.4942C>G	XP_016866593.1:p.Gln1648Glu
XM_017011105.2:c.4912C>G	XP_016866594.1:p.Gln1638Glu
XM_017011106.2:c.4783C>G	XP_016866595.1:p.Gln1595Glu
XM_017011107.2:c.4762C>G	XP_016866596.1:p.Gln1588Glu
XR_002956289.1:n.5057C>G
NM_001363725.2:c.2611C>G	NP_001350654.1:p.Gln871Glu
NM_001371656.1:c.4990C>G	NP_001358585.1:p.Gln1664Glu
NM_001374820.1:c.4990C>G	NP_001361749.1:p.Gln1664Glu
NM_001374828.1:c.5110C>G MANE Select	NP_001361757.1:p.Gln1704Glu
NM_017519.3:c.4951C>G	NP_059989.3:p.Gln1651Glu