Canonical Allele Identifier: CA366388679

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469794C>T (hg19) ; chr6:g.157148660C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148660C>T , CM000668.2:g.157148660C>T	GRCh38
NC_000006.11:g.157469794C>T , CM000668.1:g.157469794C>T	GRCh37
NC_000006.10:g.157511486C>T	NCBI36
NG_032093.1:g.375731C>T
NG_032093.2:g.375731C>T
NG_066624.1:g.377635C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2798C>T	ENSP00000055163.8:p.Pro933Leu
ENST00000414678.8:c.2708C>T	ENSP00000412835.3:p.Pro903Leu
ENST00000637015.2:c.2798C>T	ENSP00000489729.2:p.Pro933Leu
ENST00000319584.11:c.812C>T	ENSP00000313006.7:p.Pro271Leu
ENST00000346085.10:c.2837C>T	ENSP00000344546.5:p.Pro946Leu
ENST00000350026.10:c.2549C>T	ENSP00000055163.7:p.Pro850Leu
ENST00000414678.7:c.956C>T	ENSP00000412835.2:p.Pro319Leu
ENST00000452544.2:n.699C>T
ENST00000635849.1:c.119C>T	ENSP00000490948.1:p.Pro40Leu
ENST00000636930.2:c.2798C>T MANE Select	ENSP00000490491.2:p.Pro933Leu
ENST00000637015.1:c.37C>T
ENST00000637810.1:c.299C>T	ENSP00000489636.1:p.Pro100Leu
ENST00000637904.1:c.299C>T	ENSP00000490550.1:p.Pro100Leu
ENST00000647938.1:c.2588C>T	ENSP00000498155.1:p.Pro863Leu
ENST00000674190.1:n.1547C>T
ENST00000319584.10:c.815C>T	ENSP00000313006.6:p.Pro272Leu
ENST00000346085.9:c.2588C>T	ENSP00000344546.4:p.Pro863Leu
ENST00000350026.9:c.2549C>T	ENSP00000055163.7:p.Pro850Leu
ENST00000414678.6:c.956C>T	ENSP00000412835.2:p.Pro319Leu
ENST00000452544.1:n.645C>T
NM_017519.2:c.2549C>T	NP_059989.2:p.Pro850Leu
NM_020732.3:c.2588C>T	NP_065783.3:p.Pro863Leu
XM_005267069.3:c.2549C>T	XP_005267126.2:p.Pro850Leu
XM_011535984.1:c.1499C>T	XP_011534286.1:p.Pro500Leu
XM_011535985.1:c.1319C>T	XP_011534287.1:p.Pro440Leu
XM_011535986.1:c.1079C>T	XP_011534288.1:p.Pro360Leu
XM_011535987.1:c.698C>T	XP_011534289.1:p.Pro233Leu
XM_011535988.1:c.-20+15453C>T	XP_011534290.1:n.-20+15453C>T
NM_001346813.1:c.2549C>T	NP_001333742.1:p.Pro850Leu
NM_001363725.1:c.299C>T	NP_001350654.1:p.Pro100Leu
XM_011535984.2:c.2630C>T	XP_011534286.2:p.Pro877Leu
XM_011535988.3:c.-20+15453C>T	XP_011534290.1:n.-20+15453C>T
XM_017011103.2:c.2630C>T	XP_016866592.1:p.Pro877Leu
XM_017011104.1:c.2630C>T	XP_016866593.1:p.Pro877Leu
XM_017011105.2:c.2630C>T	XP_016866594.1:p.Pro877Leu
XM_017011106.2:c.2630C>T	XP_016866595.1:p.Pro877Leu
XM_017011107.2:c.2450C>T	XP_016866596.1:p.Pro817Leu
XR_002956289.1:n.2713C>T
NM_001363725.2:c.299C>T	NP_001350654.1:p.Pro100Leu
NM_001371656.1:c.2837C>T	NP_001358585.1:p.Pro946Leu
NM_001374820.1:c.2837C>T	NP_001361749.1:p.Pro946Leu
NM_001374828.1:c.2798C>T MANE Select	NP_001361757.1:p.Pro933Leu
NM_017519.3:c.2798C>T	NP_059989.3:p.Pro933Leu