Canonical Allele Identifier: CA452784760

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128376255
• MyVariant Identifiers: chr6:g.157522498C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201364C>T , CM000668.2:g.157201364C>T	GRCh38
NC_000006.11:g.157522498C>T , CM000668.1:g.157522498C>T	GRCh37
NC_000006.10:g.157564190C>T	NCBI36
NG_032093.1:g.428435C>T
NG_032093.2:g.428435C>T
NG_066624.1:g.430339C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4980C>T	ENSP00000055163.8:p.Ser1660=
ENST00000414678.8:c.5049C>T	ENSP00000412835.3:p.Ser1683=
ENST00000637015.2:c.5268C>T	ENSP00000489729.2:p.Ser1756=
ENST00000346085.10:c.5019C>T	ENSP00000344546.5:p.Ser1673=
ENST00000350026.10:c.4731C>T	ENSP00000055163.7:p.Ser1577=
ENST00000414678.7:c.3297C>T	ENSP00000412835.2:p.Ser1099=
ENST00000635849.1:c.2460C>T	ENSP00000490948.1:p.Ser820=
ENST00000635957.1:c.2091C>T	ENSP00000490385.1:p.Ser697=
ENST00000636227.1:n.3602C>T
ENST00000636254.1:n.1059C>T
ENST00000636930.2:c.5139C>T MANE Select	ENSP00000490491.2:p.Ser1713=
ENST00000636940.1:n.3136C>T
ENST00000637015.1:c.2507C>T
ENST00000637568.1:c.2421C>T
ENST00000637741.1:n.1805C>T
ENST00000637810.1:c.2481C>T	ENSP00000489636.1:p.Ser827=
ENST00000637904.1:c.2640C>T	ENSP00000490550.1:p.Ser880=
ENST00000647938.1:c.4770C>T	ENSP00000498155.1:p.Ser1590=
ENST00000346085.9:c.4770C>T	ENSP00000344546.4:p.Ser1590=
ENST00000350026.9:c.4731C>T	ENSP00000055163.7:p.Ser1577=
ENST00000414678.6:c.3297C>T	ENSP00000412835.2:p.Ser1099=
NM_017519.2:c.4731C>T	NP_059989.2:p.Ser1577=
NM_020732.3:c.4770C>T	NP_065783.3:p.Ser1590=
XM_005267069.3:c.4890C>T	XP_005267126.2:p.Ser1630=
XM_011535984.1:c.3969C>T	XP_011534286.1:p.Ser1323=
XM_011535985.1:c.3789C>T	XP_011534287.1:p.Ser1263=
XM_011535986.1:c.3549C>T	XP_011534288.1:p.Ser1183=
XM_011535987.1:c.3168C>T	XP_011534289.1:p.Ser1056=
XM_011535988.1:c.2031C>T	XP_011534290.1:p.Ser677=
NM_001346813.1:c.4890C>T	NP_001333742.1:p.Ser1630=
NM_001363725.1:c.2640C>T	NP_001350654.1:p.Ser880=
XM_011535984.2:c.5100C>T	XP_011534286.2:p.Ser1700=
XM_011535988.3:c.2031C>T	XP_011534290.1:p.Ser677=
XM_017011103.2:c.5001C>T	XP_016866592.1:p.Ser1667=
XM_017011104.1:c.4971C>T	XP_016866593.1:p.Ser1657=
XM_017011105.2:c.4941C>T	XP_016866594.1:p.Ser1647=
XM_017011106.2:c.4812C>T	XP_016866595.1:p.Ser1604=
XM_017011107.2:c.4791C>T	XP_016866596.1:p.Ser1597=
XR_002956289.1:n.5086C>T
NM_001363725.2:c.2640C>T	NP_001350654.1:p.Ser880=
NM_001371656.1:c.5019C>T	NP_001358585.1:p.Ser1673=
NM_001374820.1:c.5019C>T	NP_001361749.1:p.Ser1673=
NM_001374828.1:c.5139C>T MANE Select	NP_001361757.1:p.Ser1713=
NM_017519.3:c.4980C>T	NP_059989.3:p.Ser1660=