Canonical Allele Identifier: CA366389057

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469967C>A (hg19) ; chr6:g.157148833C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148833C>A , CM000668.2:g.157148833C>A	GRCh38
NC_000006.11:g.157469967C>A , CM000668.1:g.157469967C>A	GRCh37
NC_000006.10:g.157511659C>A	NCBI36
NG_032093.1:g.375904C>A
NG_032093.2:g.375904C>A
NG_066624.1:g.377808C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2971C>A	ENSP00000055163.8:p.Pro991Thr
ENST00000414678.8:c.2881C>A	ENSP00000412835.3:p.Pro961Thr
ENST00000637015.2:c.2971C>A	ENSP00000489729.2:p.Pro991Thr
ENST00000319584.11:c.985C>A	ENSP00000313006.7:p.Pro329Thr
ENST00000346085.10:c.3010C>A	ENSP00000344546.5:p.Pro1004Thr
ENST00000350026.10:c.2722C>A	ENSP00000055163.7:p.Pro908Thr
ENST00000414678.7:c.1129C>A	ENSP00000412835.2:p.Pro377Thr
ENST00000452544.2:n.872C>A
ENST00000635849.1:c.292C>A	ENSP00000490948.1:p.Pro98Thr
ENST00000636426.1:n.105C>A
ENST00000636930.2:c.2971C>A MANE Select	ENSP00000490491.2:p.Pro991Thr
ENST00000637015.1:c.210C>A
ENST00000637568.1:c.14C>A
ENST00000637810.1:c.472C>A	ENSP00000489636.1:p.Pro158Thr
ENST00000637904.1:c.472C>A	ENSP00000490550.1:p.Pro158Thr
ENST00000647938.1:c.2761C>A	ENSP00000498155.1:p.Pro921Thr
ENST00000674190.1:n.1720C>A
ENST00000319584.10:c.988C>A	ENSP00000313006.6:p.Pro330Thr
ENST00000346085.9:c.2761C>A	ENSP00000344546.4:p.Pro921Thr
ENST00000350026.9:c.2722C>A	ENSP00000055163.7:p.Pro908Thr
ENST00000414678.6:c.1129C>A	ENSP00000412835.2:p.Pro377Thr
ENST00000452544.1:n.818C>A
ENST00000478761.3:c.44C>A
NM_017519.2:c.2722C>A	NP_059989.2:p.Pro908Thr
NM_020732.3:c.2761C>A	NP_065783.3:p.Pro921Thr
XM_005267069.3:c.2722C>A	XP_005267126.2:p.Pro908Thr
XM_011535984.1:c.1672C>A	XP_011534286.1:p.Pro558Thr
XM_011535985.1:c.1492C>A	XP_011534287.1:p.Pro498Thr
XM_011535986.1:c.1252C>A	XP_011534288.1:p.Pro418Thr
XM_011535987.1:c.871C>A	XP_011534289.1:p.Pro291Thr
XM_011535988.1:c.-20+15626C>A	XP_011534290.1:n.-20+15626C>A
NM_001346813.1:c.2722C>A	NP_001333742.1:p.Pro908Thr
NM_001363725.1:c.472C>A	NP_001350654.1:p.Pro158Thr
XM_011535984.2:c.2803C>A	XP_011534286.2:p.Pro935Thr
XM_011535988.3:c.-20+15626C>A	XP_011534290.1:n.-20+15626C>A
XM_017011103.2:c.2803C>A	XP_016866592.1:p.Pro935Thr
XM_017011104.1:c.2803C>A	XP_016866593.1:p.Pro935Thr
XM_017011105.2:c.2803C>A	XP_016866594.1:p.Pro935Thr
XM_017011106.2:c.2803C>A	XP_016866595.1:p.Pro935Thr
XM_017011107.2:c.2623C>A	XP_016866596.1:p.Pro875Thr
XR_002956289.1:n.2886C>A
NM_001363725.2:c.472C>A	NP_001350654.1:p.Pro158Thr
NM_001371656.1:c.3010C>A	NP_001358585.1:p.Pro1004Thr
NM_001374820.1:c.3010C>A	NP_001361749.1:p.Pro1004Thr
NM_001374828.1:c.2971C>A MANE Select	NP_001361757.1:p.Pro991Thr
NM_017519.3:c.2971C>A	NP_059989.3:p.Pro991Thr