Canonical Allele Identifier: CA452780773

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128317195
• MyVariant Identifiers: chr6:g.157502204C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181070C>T , CM000668.2:g.157181070C>T	GRCh38
NC_000006.11:g.157502204C>T , CM000668.1:g.157502204C>T	GRCh37
NC_000006.10:g.157543896C>T	NCBI36
NG_032093.1:g.408141C>T
NG_032093.2:g.408141C>T
NG_066624.1:g.410045C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3447C>T	ENSP00000055163.8:p.Phe1149=
ENST00000414678.8:c.3516C>T	ENSP00000412835.3:p.Phe1172=
ENST00000637015.2:c.3735C>T	ENSP00000489729.2:p.Phe1245=
ENST00000319584.11:c.1620C>T	ENSP00000313006.7:p.Phe540=
ENST00000346085.10:c.3486C>T	ENSP00000344546.5:p.Phe1162=
ENST00000350026.10:c.3198C>T	ENSP00000055163.7:p.Phe1066=
ENST00000414678.7:c.1764C>T	ENSP00000412835.2:p.Phe588=
ENST00000635849.1:c.927C>T	ENSP00000490948.1:p.Phe309=
ENST00000635957.1:c.561C>T	ENSP00000490385.1:p.Phe187=
ENST00000636930.2:c.3606C>T MANE Select	ENSP00000490491.2:p.Phe1202=
ENST00000636940.1:n.1603C>T
ENST00000637015.1:c.974C>T
ENST00000637568.1:c.888C>T
ENST00000637741.1:n.272C>T
ENST00000637810.1:c.948C>T	ENSP00000489636.1:p.Phe316=
ENST00000637904.1:c.1107C>T	ENSP00000490550.1:p.Phe369=
ENST00000647938.1:c.3237C>T	ENSP00000498155.1:p.Phe1079=
ENST00000319584.10:c.1623C>T	ENSP00000313006.6:p.Phe541=
ENST00000346085.9:c.3237C>T	ENSP00000344546.4:p.Phe1079=
ENST00000350026.9:c.3198C>T	ENSP00000055163.7:p.Phe1066=
ENST00000400790.3:c.399C>T	ENSP00000383596.3:p.Phe133=
ENST00000414678.6:c.1764C>T	ENSP00000412835.2:p.Phe588=
ENST00000478761.3:c.808C>T
NM_017519.2:c.3198C>T	NP_059989.2:p.Phe1066=
NM_020732.3:c.3237C>T	NP_065783.3:p.Phe1079=
XM_005267069.3:c.3357C>T	XP_005267126.2:p.Phe1119=
XM_011535984.1:c.2436C>T	XP_011534286.1:p.Phe812=
XM_011535985.1:c.2256C>T	XP_011534287.1:p.Phe752=
XM_011535986.1:c.2016C>T	XP_011534288.1:p.Phe672=
XM_011535987.1:c.1635C>T	XP_011534289.1:p.Phe545=
XM_011535988.1:c.498C>T	XP_011534290.1:p.Phe166=
NM_001346813.1:c.3357C>T	NP_001333742.1:p.Phe1119=
NM_001363725.1:c.1107C>T	NP_001350654.1:p.Phe369=
XM_011535984.2:c.3567C>T	XP_011534286.2:p.Phe1189=
XM_011535988.3:c.498C>T	XP_011534290.1:p.Phe166=
XM_017011103.2:c.3468C>T	XP_016866592.1:p.Phe1156=
XM_017011104.1:c.3438C>T	XP_016866593.1:p.Phe1146=
XM_017011105.2:c.3408C>T	XP_016866594.1:p.Phe1136=
XM_017011106.2:c.3279C>T	XP_016866595.1:p.Phe1093=
XM_017011107.2:c.3258C>T	XP_016866596.1:p.Phe1086=
XR_002956289.1:n.3650C>T
NM_001363725.2:c.1107C>T	NP_001350654.1:p.Phe369=
NM_001371656.1:c.3486C>T	NP_001358585.1:p.Phe1162=
NM_001374820.1:c.3486C>T	NP_001361749.1:p.Phe1162=
NM_001374828.1:c.3606C>T MANE Select	NP_001361757.1:p.Phe1202=
NM_017519.3:c.3447C>T	NP_059989.3:p.Phe1149=