Canonical Allele Identifier: CA366241726

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522187G>T (hg19) ; chr6:g.157201053G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201053G>T , CM000668.2:g.157201053G>T	GRCh38
NC_000006.11:g.157522187G>T , CM000668.1:g.157522187G>T	GRCh37
NC_000006.10:g.157563879G>T	NCBI36
NG_032093.1:g.428124G>T
NG_032093.2:g.428124G>T
NG_066624.1:g.430028G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4669G>T	ENSP00000055163.8:p.Ala1557Ser
ENST00000414678.8:c.4738G>T	ENSP00000412835.3:p.Ala1580Ser
ENST00000637015.2:c.4957G>T	ENSP00000489729.2:p.Ala1653Ser
ENST00000346085.10:c.4708G>T	ENSP00000344546.5:p.Ala1570Ser
ENST00000350026.10:c.4420G>T	ENSP00000055163.7:p.Ala1474Ser
ENST00000414678.7:c.2986G>T	ENSP00000412835.2:p.Ala996Ser
ENST00000635849.1:c.2149G>T	ENSP00000490948.1:p.Ala717Ser
ENST00000635957.1:c.1780G>T	ENSP00000490385.1:p.Ala594Ser
ENST00000636227.1:n.3291G>T
ENST00000636254.1:n.748G>T
ENST00000636930.2:c.4828G>T MANE Select	ENSP00000490491.2:p.Ala1610Ser
ENST00000636940.1:n.2825G>T
ENST00000637015.1:c.2196G>T
ENST00000637568.1:c.2110G>T
ENST00000637741.1:n.1494G>T
ENST00000637810.1:c.2170G>T	ENSP00000489636.1:p.Ala724Ser
ENST00000637904.1:c.2329G>T	ENSP00000490550.1:p.Ala777Ser
ENST00000647938.1:c.4459G>T	ENSP00000498155.1:p.Ala1487Ser
ENST00000346085.9:c.4459G>T	ENSP00000344546.4:p.Ala1487Ser
ENST00000350026.9:c.4420G>T	ENSP00000055163.7:p.Ala1474Ser
ENST00000414678.6:c.2986G>T	ENSP00000412835.2:p.Ala996Ser
NM_017519.2:c.4420G>T	NP_059989.2:p.Ala1474Ser
NM_020732.3:c.4459G>T	NP_065783.3:p.Ala1487Ser
XM_005267069.3:c.4579G>T	XP_005267126.2:p.Ala1527Ser
XM_011535984.1:c.3658G>T	XP_011534286.1:p.Ala1220Ser
XM_011535985.1:c.3478G>T	XP_011534287.1:p.Ala1160Ser
XM_011535986.1:c.3238G>T	XP_011534288.1:p.Ala1080Ser
XM_011535987.1:c.2857G>T	XP_011534289.1:p.Ala953Ser
XM_011535988.1:c.1720G>T	XP_011534290.1:p.Ala574Ser
NM_001346813.1:c.4579G>T	NP_001333742.1:p.Ala1527Ser
NM_001363725.1:c.2329G>T	NP_001350654.1:p.Ala777Ser
XM_011535984.2:c.4789G>T	XP_011534286.2:p.Ala1597Ser
XM_011535988.3:c.1720G>T	XP_011534290.1:p.Ala574Ser
XM_017011103.2:c.4690G>T	XP_016866592.1:p.Ala1564Ser
XM_017011104.1:c.4660G>T	XP_016866593.1:p.Ala1554Ser
XM_017011105.2:c.4630G>T	XP_016866594.1:p.Ala1544Ser
XM_017011106.2:c.4501G>T	XP_016866595.1:p.Ala1501Ser
XM_017011107.2:c.4480G>T	XP_016866596.1:p.Ala1494Ser
XR_002956289.1:n.4775G>T
NM_001363725.2:c.2329G>T	NP_001350654.1:p.Ala777Ser
NM_001371656.1:c.4708G>T	NP_001358585.1:p.Ala1570Ser
NM_001374820.1:c.4708G>T	NP_001361749.1:p.Ala1570Ser
NM_001374828.1:c.4828G>T MANE Select	NP_001361757.1:p.Ala1610Ser
NM_017519.3:c.4669G>T	NP_059989.3:p.Ala1557Ser