Canonical Allele Identifier: CA366242436

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522433C>T (hg19) ; chr6:g.157201299C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201299C>T , CM000668.2:g.157201299C>T	GRCh38
NC_000006.11:g.157522433C>T , CM000668.1:g.157522433C>T	GRCh37
NC_000006.10:g.157564125C>T	NCBI36
NG_032093.1:g.428370C>T
NG_032093.2:g.428370C>T
NG_066624.1:g.430274C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4915C>T	ENSP00000055163.8:p.Pro1639Ser
ENST00000414678.8:c.4984C>T	ENSP00000412835.3:p.Pro1662Ser
ENST00000637015.2:c.5203C>T	ENSP00000489729.2:p.Pro1735Ser
ENST00000346085.10:c.4954C>T	ENSP00000344546.5:p.Pro1652Ser
ENST00000350026.10:c.4666C>T	ENSP00000055163.7:p.Pro1556Ser
ENST00000414678.7:c.3232C>T	ENSP00000412835.2:p.Pro1078Ser
ENST00000635849.1:c.2395C>T	ENSP00000490948.1:p.Pro799Ser
ENST00000635957.1:c.2026C>T	ENSP00000490385.1:p.Pro676Ser
ENST00000636227.1:n.3537C>T
ENST00000636254.1:n.994C>T
ENST00000636930.2:c.5074C>T MANE Select	ENSP00000490491.2:p.Pro1692Ser
ENST00000636940.1:n.3071C>T
ENST00000637015.1:c.2442C>T
ENST00000637568.1:c.2356C>T
ENST00000637741.1:n.1740C>T
ENST00000637810.1:c.2416C>T	ENSP00000489636.1:p.Pro806Ser
ENST00000637904.1:c.2575C>T	ENSP00000490550.1:p.Pro859Ser
ENST00000647938.1:c.4705C>T	ENSP00000498155.1:p.Pro1569Ser
ENST00000346085.9:c.4705C>T	ENSP00000344546.4:p.Pro1569Ser
ENST00000350026.9:c.4666C>T	ENSP00000055163.7:p.Pro1556Ser
ENST00000414678.6:c.3232C>T	ENSP00000412835.2:p.Pro1078Ser
NM_017519.2:c.4666C>T	NP_059989.2:p.Pro1556Ser
NM_020732.3:c.4705C>T	NP_065783.3:p.Pro1569Ser
XM_005267069.3:c.4825C>T	XP_005267126.2:p.Pro1609Ser
XM_011535984.1:c.3904C>T	XP_011534286.1:p.Pro1302Ser
XM_011535985.1:c.3724C>T	XP_011534287.1:p.Pro1242Ser
XM_011535986.1:c.3484C>T	XP_011534288.1:p.Pro1162Ser
XM_011535987.1:c.3103C>T	XP_011534289.1:p.Pro1035Ser
XM_011535988.1:c.1966C>T	XP_011534290.1:p.Pro656Ser
NM_001346813.1:c.4825C>T	NP_001333742.1:p.Pro1609Ser
NM_001363725.1:c.2575C>T	NP_001350654.1:p.Pro859Ser
XM_011535984.2:c.5035C>T	XP_011534286.2:p.Pro1679Ser
XM_011535988.3:c.1966C>T	XP_011534290.1:p.Pro656Ser
XM_017011103.2:c.4936C>T	XP_016866592.1:p.Pro1646Ser
XM_017011104.1:c.4906C>T	XP_016866593.1:p.Pro1636Ser
XM_017011105.2:c.4876C>T	XP_016866594.1:p.Pro1626Ser
XM_017011106.2:c.4747C>T	XP_016866595.1:p.Pro1583Ser
XM_017011107.2:c.4726C>T	XP_016866596.1:p.Pro1576Ser
XR_002956289.1:n.5021C>T
NM_001363725.2:c.2575C>T	NP_001350654.1:p.Pro859Ser
NM_001371656.1:c.4954C>T	NP_001358585.1:p.Pro1652Ser
NM_001374820.1:c.4954C>T	NP_001361749.1:p.Pro1652Ser
NM_001374828.1:c.5074C>T MANE Select	NP_001361757.1:p.Pro1692Ser
NM_017519.3:c.4915C>T	NP_059989.3:p.Pro1639Ser