Canonical Allele Identifier: CA452990262

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469960C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148826C>A , CM000668.2:g.157148826C>A	GRCh38
NC_000006.11:g.157469960C>A , CM000668.1:g.157469960C>A	GRCh37
NC_000006.10:g.157511652C>A	NCBI36
NG_032093.1:g.375897C>A
NG_032093.2:g.375897C>A
NG_066624.1:g.377801C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2964C>A	ENSP00000055163.8:p.Pro988=
ENST00000414678.8:c.2874C>A	ENSP00000412835.3:p.Pro958=
ENST00000637015.2:c.2964C>A	ENSP00000489729.2:p.Pro988=
ENST00000319584.11:c.978C>A	ENSP00000313006.7:p.Pro326=
ENST00000346085.10:c.3003C>A	ENSP00000344546.5:p.Pro1001=
ENST00000350026.10:c.2715C>A	ENSP00000055163.7:p.Pro905=
ENST00000414678.7:c.1122C>A	ENSP00000412835.2:p.Pro374=
ENST00000452544.2:n.865C>A
ENST00000635849.1:c.285C>A	ENSP00000490948.1:p.Pro95=
ENST00000636426.1:n.98C>A
ENST00000636930.2:c.2964C>A MANE Select	ENSP00000490491.2:p.Pro988=
ENST00000637015.1:c.203C>A
ENST00000637568.1:c.7C>A
ENST00000637810.1:c.465C>A	ENSP00000489636.1:p.Pro155=
ENST00000637904.1:c.465C>A	ENSP00000490550.1:p.Pro155=
ENST00000647938.1:c.2754C>A	ENSP00000498155.1:p.Pro918=
ENST00000674190.1:n.1713C>A
ENST00000319584.10:c.981C>A	ENSP00000313006.6:p.Pro327=
ENST00000346085.9:c.2754C>A	ENSP00000344546.4:p.Pro918=
ENST00000350026.9:c.2715C>A	ENSP00000055163.7:p.Pro905=
ENST00000414678.6:c.1122C>A	ENSP00000412835.2:p.Pro374=
ENST00000452544.1:n.811C>A
ENST00000478761.3:c.37C>A
NM_017519.2:c.2715C>A	NP_059989.2:p.Pro905=
NM_020732.3:c.2754C>A	NP_065783.3:p.Pro918=
XM_005267069.3:c.2715C>A	XP_005267126.2:p.Pro905=
XM_011535984.1:c.1665C>A	XP_011534286.1:p.Pro555=
XM_011535985.1:c.1485C>A	XP_011534287.1:p.Pro495=
XM_011535986.1:c.1245C>A	XP_011534288.1:p.Pro415=
XM_011535987.1:c.864C>A	XP_011534289.1:p.Pro288=
XM_011535988.1:c.-20+15619C>A	XP_011534290.1:n.-20+15619C>A
NM_001346813.1:c.2715C>A	NP_001333742.1:p.Pro905=
NM_001363725.1:c.465C>A	NP_001350654.1:p.Pro155=
XM_011535984.2:c.2796C>A	XP_011534286.2:p.Pro932=
XM_011535988.3:c.-20+15619C>A	XP_011534290.1:n.-20+15619C>A
XM_017011103.2:c.2796C>A	XP_016866592.1:p.Pro932=
XM_017011104.1:c.2796C>A	XP_016866593.1:p.Pro932=
XM_017011105.2:c.2796C>A	XP_016866594.1:p.Pro932=
XM_017011106.2:c.2796C>A	XP_016866595.1:p.Pro932=
XM_017011107.2:c.2616C>A	XP_016866596.1:p.Pro872=
XR_002956289.1:n.2879C>A
NM_001363725.2:c.465C>A	NP_001350654.1:p.Pro155=
NM_001371656.1:c.3003C>A	NP_001358585.1:p.Pro1001=
NM_001374820.1:c.3003C>A	NP_001361749.1:p.Pro1001=
NM_001374828.1:c.2964C>A MANE Select	NP_001361757.1:p.Pro988=
NM_017519.3:c.2964C>A	NP_059989.3:p.Pro988=