Canonical Allele Identifier: CA366234140

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3830C>A	ENSP00000055163.8:p.Pro1277Gln
ENST00000414678.8:c.3899C>A	ENSP00000412835.3:p.Pro1300Gln
ENST00000637015.2:c.4118C>A	ENSP00000489729.2:p.Pro1373Gln
ENST00000346085.10:c.3869C>A	ENSP00000344546.5:p.Pro1290Gln
ENST00000350026.10:c.3581C>A	ENSP00000055163.7:p.Pro1194Gln
ENST00000414678.7:c.2147C>A	ENSP00000412835.2:p.Pro716Gln
ENST00000635849.1:c.1310C>A	ENSP00000490948.1:p.Pro437Gln
ENST00000635957.1:c.944C>A	ENSP00000490385.1:p.Pro315Gln
ENST00000636930.2:c.3989C>A MANE Select	ENSP00000490491.2:p.Pro1330Gln
ENST00000636940.1:n.1986C>A
ENST00000637015.1:c.1357C>A
ENST00000637568.1:c.1271C>A
ENST00000637741.1:n.655C>A
ENST00000637810.1:c.1331C>A	ENSP00000489636.1:p.Pro444Gln
ENST00000637904.1:c.1490C>A	ENSP00000490550.1:p.Pro497Gln
ENST00000647938.1:c.3620C>A	ENSP00000498155.1:p.Pro1207Gln
ENST00000346085.9:c.3620C>A	ENSP00000344546.4:p.Pro1207Gln
ENST00000350026.9:c.3581C>A	ENSP00000055163.7:p.Pro1194Gln
ENST00000414678.6:c.2147C>A	ENSP00000412835.2:p.Pro716Gln
NM_017519.2:c.3581C>A	NP_059989.2:p.Pro1194Gln
NM_020732.3:c.3620C>A	NP_065783.3:p.Pro1207Gln
XM_005267069.3:c.3740C>A	XP_005267126.2:p.Pro1247Gln
XM_011535984.1:c.2819C>A	XP_011534286.1:p.Pro940Gln
XM_011535985.1:c.2639C>A	XP_011534287.1:p.Pro880Gln
XM_011535986.1:c.2399C>A	XP_011534288.1:p.Pro800Gln
XM_011535987.1:c.2018C>A	XP_011534289.1:p.Pro673Gln
XM_011535988.1:c.881C>A	XP_011534290.1:p.Pro294Gln
NM_001346813.1:c.3740C>A	NP_001333742.1:p.Pro1247Gln
NM_001363725.1:c.1490C>A	NP_001350654.1:p.Pro497Gln
XM_011535984.2:c.3950C>A	XP_011534286.2:p.Pro1317Gln
XM_011535988.3:c.881C>A	XP_011534290.1:p.Pro294Gln
XM_017011103.2:c.3851C>A	XP_016866592.1:p.Pro1284Gln
XM_017011104.1:c.3821C>A	XP_016866593.1:p.Pro1274Gln
XM_017011105.2:c.3791C>A	XP_016866594.1:p.Pro1264Gln
XM_017011106.2:c.3662C>A	XP_016866595.1:p.Pro1221Gln
XM_017011107.2:c.3641C>A	XP_016866596.1:p.Pro1214Gln
XR_002956289.1:n.4033C>A
NM_001363725.2:c.1490C>A	NP_001350654.1:p.Pro497Gln
NM_001371656.1:c.3869C>A	NP_001358585.1:p.Pro1290Gln
NM_001374820.1:c.3869C>A	NP_001361749.1:p.Pro1290Gln
NM_001374828.1:c.3989C>A MANE Select	NP_001361757.1:p.Pro1330Gln
NM_017519.3:c.3830C>A	NP_059989.3:p.Pro1277Gln