Canonical Allele Identifier: CA366389058

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2971C>G	ENSP00000055163.8:p.Pro991Ala
ENST00000414678.8:c.2881C>G	ENSP00000412835.3:p.Pro961Ala
ENST00000637015.2:c.2971C>G	ENSP00000489729.2:p.Pro991Ala
ENST00000319584.11:c.985C>G	ENSP00000313006.7:p.Pro329Ala
ENST00000346085.10:c.3010C>G	ENSP00000344546.5:p.Pro1004Ala
ENST00000350026.10:c.2722C>G	ENSP00000055163.7:p.Pro908Ala
ENST00000414678.7:c.1129C>G	ENSP00000412835.2:p.Pro377Ala
ENST00000452544.2:n.872C>G
ENST00000635849.1:c.292C>G	ENSP00000490948.1:p.Pro98Ala
ENST00000636426.1:n.105C>G
ENST00000636930.2:c.2971C>G MANE Select	ENSP00000490491.2:p.Pro991Ala
ENST00000637015.1:c.210C>G
ENST00000637568.1:c.14C>G
ENST00000637810.1:c.472C>G	ENSP00000489636.1:p.Pro158Ala
ENST00000637904.1:c.472C>G	ENSP00000490550.1:p.Pro158Ala
ENST00000647938.1:c.2761C>G	ENSP00000498155.1:p.Pro921Ala
ENST00000674190.1:n.1720C>G
ENST00000319584.10:c.988C>G	ENSP00000313006.6:p.Pro330Ala
ENST00000346085.9:c.2761C>G	ENSP00000344546.4:p.Pro921Ala
ENST00000350026.9:c.2722C>G	ENSP00000055163.7:p.Pro908Ala
ENST00000414678.6:c.1129C>G	ENSP00000412835.2:p.Pro377Ala
ENST00000452544.1:n.818C>G
ENST00000478761.3:c.44C>G
NM_017519.2:c.2722C>G	NP_059989.2:p.Pro908Ala
NM_020732.3:c.2761C>G	NP_065783.3:p.Pro921Ala
XM_005267069.3:c.2722C>G	XP_005267126.2:p.Pro908Ala
XM_011535984.1:c.1672C>G	XP_011534286.1:p.Pro558Ala
XM_011535985.1:c.1492C>G	XP_011534287.1:p.Pro498Ala
XM_011535986.1:c.1252C>G	XP_011534288.1:p.Pro418Ala
XM_011535987.1:c.871C>G	XP_011534289.1:p.Pro291Ala
XM_011535988.1:c.-20+15626C>G	XP_011534290.1:n.-20+15626C>G
NM_001346813.1:c.2722C>G	NP_001333742.1:p.Pro908Ala
NM_001363725.1:c.472C>G	NP_001350654.1:p.Pro158Ala
XM_011535984.2:c.2803C>G	XP_011534286.2:p.Pro935Ala
XM_011535988.3:c.-20+15626C>G	XP_011534290.1:n.-20+15626C>G
XM_017011103.2:c.2803C>G	XP_016866592.1:p.Pro935Ala
XM_017011104.1:c.2803C>G	XP_016866593.1:p.Pro935Ala
XM_017011105.2:c.2803C>G	XP_016866594.1:p.Pro935Ala
XM_017011106.2:c.2803C>G	XP_016866595.1:p.Pro935Ala
XM_017011107.2:c.2623C>G	XP_016866596.1:p.Pro875Ala
XR_002956289.1:n.2886C>G
NM_001363725.2:c.472C>G	NP_001350654.1:p.Pro158Ala
NM_001371656.1:c.3010C>G	NP_001358585.1:p.Pro1004Ala
NM_001374820.1:c.3010C>G	NP_001361749.1:p.Pro1004Ala
NM_001374828.1:c.2971C>G MANE Select	NP_001361757.1:p.Pro991Ala
NM_017519.3:c.2971C>G	NP_059989.3:p.Pro991Ala