Canonical Allele Identifier: CA366234141

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510845C>G (hg19) ; chr6:g.157189711C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189711C>G , CM000668.2:g.157189711C>G	GRCh38
NC_000006.11:g.157510845C>G , CM000668.1:g.157510845C>G	GRCh37
NC_000006.10:g.157552537C>G	NCBI36
NG_032093.1:g.416782C>G
NG_032093.2:g.416782C>G
NG_066624.1:g.418686C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3830C>G	ENSP00000055163.8:p.Pro1277Arg
ENST00000414678.8:c.3899C>G	ENSP00000412835.3:p.Pro1300Arg
ENST00000637015.2:c.4118C>G	ENSP00000489729.2:p.Pro1373Arg
ENST00000346085.10:c.3869C>G	ENSP00000344546.5:p.Pro1290Arg
ENST00000350026.10:c.3581C>G	ENSP00000055163.7:p.Pro1194Arg
ENST00000414678.7:c.2147C>G	ENSP00000412835.2:p.Pro716Arg
ENST00000635849.1:c.1310C>G	ENSP00000490948.1:p.Pro437Arg
ENST00000635957.1:c.944C>G	ENSP00000490385.1:p.Pro315Arg
ENST00000636930.2:c.3989C>G MANE Select	ENSP00000490491.2:p.Pro1330Arg
ENST00000636940.1:n.1986C>G
ENST00000637015.1:c.1357C>G
ENST00000637568.1:c.1271C>G
ENST00000637741.1:n.655C>G
ENST00000637810.1:c.1331C>G	ENSP00000489636.1:p.Pro444Arg
ENST00000637904.1:c.1490C>G	ENSP00000490550.1:p.Pro497Arg
ENST00000647938.1:c.3620C>G	ENSP00000498155.1:p.Pro1207Arg
ENST00000346085.9:c.3620C>G	ENSP00000344546.4:p.Pro1207Arg
ENST00000350026.9:c.3581C>G	ENSP00000055163.7:p.Pro1194Arg
ENST00000414678.6:c.2147C>G	ENSP00000412835.2:p.Pro716Arg
NM_017519.2:c.3581C>G	NP_059989.2:p.Pro1194Arg
NM_020732.3:c.3620C>G	NP_065783.3:p.Pro1207Arg
XM_005267069.3:c.3740C>G	XP_005267126.2:p.Pro1247Arg
XM_011535984.1:c.2819C>G	XP_011534286.1:p.Pro940Arg
XM_011535985.1:c.2639C>G	XP_011534287.1:p.Pro880Arg
XM_011535986.1:c.2399C>G	XP_011534288.1:p.Pro800Arg
XM_011535987.1:c.2018C>G	XP_011534289.1:p.Pro673Arg
XM_011535988.1:c.881C>G	XP_011534290.1:p.Pro294Arg
NM_001346813.1:c.3740C>G	NP_001333742.1:p.Pro1247Arg
NM_001363725.1:c.1490C>G	NP_001350654.1:p.Pro497Arg
XM_011535984.2:c.3950C>G	XP_011534286.2:p.Pro1317Arg
XM_011535988.3:c.881C>G	XP_011534290.1:p.Pro294Arg
XM_017011103.2:c.3851C>G	XP_016866592.1:p.Pro1284Arg
XM_017011104.1:c.3821C>G	XP_016866593.1:p.Pro1274Arg
XM_017011105.2:c.3791C>G	XP_016866594.1:p.Pro1264Arg
XM_017011106.2:c.3662C>G	XP_016866595.1:p.Pro1221Arg
XM_017011107.2:c.3641C>G	XP_016866596.1:p.Pro1214Arg
XR_002956289.1:n.4033C>G
NM_001363725.2:c.1490C>G	NP_001350654.1:p.Pro497Arg
NM_001371656.1:c.3869C>G	NP_001358585.1:p.Pro1290Arg
NM_001374820.1:c.3869C>G	NP_001361749.1:p.Pro1290Arg
NM_001374828.1:c.3989C>G MANE Select	NP_001361757.1:p.Pro1330Arg
NM_017519.3:c.3830C>G	NP_059989.3:p.Pro1277Arg