Canonical Allele Identifier: CA452781511

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157189676-C-T
• MyVariant Identifiers: chr6:g.157510810C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189676C>T , CM000668.2:g.157189676C>T	GRCh38
NC_000006.11:g.157510810C>T , CM000668.1:g.157510810C>T	GRCh37
NC_000006.10:g.157552502C>T	NCBI36
NG_032093.1:g.416747C>T
NG_032093.2:g.416747C>T
NG_066624.1:g.418651C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3795C>T	ENSP00000055163.8:p.Pro1265=
ENST00000414678.8:c.3864C>T	ENSP00000412835.3:p.Pro1288=
ENST00000637015.2:c.4083C>T	ENSP00000489729.2:p.Pro1361=
ENST00000346085.10:c.3834C>T	ENSP00000344546.5:p.Pro1278=
ENST00000350026.10:c.3546C>T	ENSP00000055163.7:p.Pro1182=
ENST00000414678.7:c.2112C>T	ENSP00000412835.2:p.Pro704=
ENST00000635849.1:c.1275C>T	ENSP00000490948.1:p.Pro425=
ENST00000635957.1:c.909C>T	ENSP00000490385.1:p.Pro303=
ENST00000636930.2:c.3954C>T MANE Select	ENSP00000490491.2:p.Pro1318=
ENST00000636940.1:n.1951C>T
ENST00000637015.1:c.1322C>T
ENST00000637568.1:c.1236C>T
ENST00000637741.1:n.620C>T
ENST00000637810.1:c.1296C>T	ENSP00000489636.1:p.Pro432=
ENST00000637904.1:c.1455C>T	ENSP00000490550.1:p.Pro485=
ENST00000647938.1:c.3585C>T	ENSP00000498155.1:p.Pro1195=
ENST00000346085.9:c.3585C>T	ENSP00000344546.4:p.Pro1195=
ENST00000350026.9:c.3546C>T	ENSP00000055163.7:p.Pro1182=
ENST00000414678.6:c.2112C>T	ENSP00000412835.2:p.Pro704=
NM_017519.2:c.3546C>T	NP_059989.2:p.Pro1182=
NM_020732.3:c.3585C>T	NP_065783.3:p.Pro1195=
XM_005267069.3:c.3705C>T	XP_005267126.2:p.Pro1235=
XM_011535984.1:c.2784C>T	XP_011534286.1:p.Pro928=
XM_011535985.1:c.2604C>T	XP_011534287.1:p.Pro868=
XM_011535986.1:c.2364C>T	XP_011534288.1:p.Pro788=
XM_011535987.1:c.1983C>T	XP_011534289.1:p.Pro661=
XM_011535988.1:c.846C>T	XP_011534290.1:p.Pro282=
NM_001346813.1:c.3705C>T	NP_001333742.1:p.Pro1235=
NM_001363725.1:c.1455C>T	NP_001350654.1:p.Pro485=
XM_011535984.2:c.3915C>T	XP_011534286.2:p.Pro1305=
XM_011535988.3:c.846C>T	XP_011534290.1:p.Pro282=
XM_017011103.2:c.3816C>T	XP_016866592.1:p.Pro1272=
XM_017011104.1:c.3786C>T	XP_016866593.1:p.Pro1262=
XM_017011105.2:c.3756C>T	XP_016866594.1:p.Pro1252=
XM_017011106.2:c.3627C>T	XP_016866595.1:p.Pro1209=
XM_017011107.2:c.3606C>T	XP_016866596.1:p.Pro1202=
XR_002956289.1:n.3998C>T
NM_001363725.2:c.1455C>T	NP_001350654.1:p.Pro485=
NM_001371656.1:c.3834C>T	NP_001358585.1:p.Pro1278=
NM_001374820.1:c.3834C>T	NP_001361749.1:p.Pro1278=
NM_001374828.1:c.3954C>T MANE Select	NP_001361757.1:p.Pro1318=
NM_017519.3:c.3795C>T	NP_059989.3:p.Pro1265=