Canonical Allele Identifier: CA366388914

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469904C>A (hg19) ; chr6:g.157148770C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148770C>A , CM000668.2:g.157148770C>A	GRCh38
NC_000006.11:g.157469904C>A , CM000668.1:g.157469904C>A	GRCh37
NC_000006.10:g.157511596C>A	NCBI36
NG_032093.1:g.375841C>A
NG_032093.2:g.375841C>A
NG_066624.1:g.377745C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2908C>A	ENSP00000055163.8:p.Pro970Thr
ENST00000414678.8:c.2818C>A	ENSP00000412835.3:p.Pro940Thr
ENST00000637015.2:c.2908C>A	ENSP00000489729.2:p.Pro970Thr
ENST00000319584.11:c.922C>A	ENSP00000313006.7:p.Pro308Thr
ENST00000346085.10:c.2947C>A	ENSP00000344546.5:p.Pro983Thr
ENST00000350026.10:c.2659C>A	ENSP00000055163.7:p.Pro887Thr
ENST00000414678.7:c.1066C>A	ENSP00000412835.2:p.Pro356Thr
ENST00000452544.2:n.809C>A
ENST00000635849.1:c.229C>A	ENSP00000490948.1:p.Pro77Thr
ENST00000636426.1:n.42C>A
ENST00000636930.2:c.2908C>A MANE Select	ENSP00000490491.2:p.Pro970Thr
ENST00000637015.1:c.147C>A
ENST00000637810.1:c.409C>A	ENSP00000489636.1:p.Pro137Thr
ENST00000637904.1:c.409C>A	ENSP00000490550.1:p.Pro137Thr
ENST00000647938.1:c.2698C>A	ENSP00000498155.1:p.Pro900Thr
ENST00000674190.1:n.1657C>A
ENST00000319584.10:c.925C>A	ENSP00000313006.6:p.Pro309Thr
ENST00000346085.9:c.2698C>A	ENSP00000344546.4:p.Pro900Thr
ENST00000350026.9:c.2659C>A	ENSP00000055163.7:p.Pro887Thr
ENST00000414678.6:c.1066C>A	ENSP00000412835.2:p.Pro356Thr
ENST00000452544.1:n.755C>A
NM_017519.2:c.2659C>A	NP_059989.2:p.Pro887Thr
NM_020732.3:c.2698C>A	NP_065783.3:p.Pro900Thr
XM_005267069.3:c.2659C>A	XP_005267126.2:p.Pro887Thr
XM_011535984.1:c.1609C>A	XP_011534286.1:p.Pro537Thr
XM_011535985.1:c.1429C>A	XP_011534287.1:p.Pro477Thr
XM_011535986.1:c.1189C>A	XP_011534288.1:p.Pro397Thr
XM_011535987.1:c.808C>A	XP_011534289.1:p.Pro270Thr
XM_011535988.1:c.-20+15563C>A	XP_011534290.1:n.-20+15563C>A
NM_001346813.1:c.2659C>A	NP_001333742.1:p.Pro887Thr
NM_001363725.1:c.409C>A	NP_001350654.1:p.Pro137Thr
XM_011535984.2:c.2740C>A	XP_011534286.2:p.Pro914Thr
XM_011535988.3:c.-20+15563C>A	XP_011534290.1:n.-20+15563C>A
XM_017011103.2:c.2740C>A	XP_016866592.1:p.Pro914Thr
XM_017011104.1:c.2740C>A	XP_016866593.1:p.Pro914Thr
XM_017011105.2:c.2740C>A	XP_016866594.1:p.Pro914Thr
XM_017011106.2:c.2740C>A	XP_016866595.1:p.Pro914Thr
XM_017011107.2:c.2560C>A	XP_016866596.1:p.Pro854Thr
XR_002956289.1:n.2823C>A
NM_001363725.2:c.409C>A	NP_001350654.1:p.Pro137Thr
NM_001371656.1:c.2947C>A	NP_001358585.1:p.Pro983Thr
NM_001374820.1:c.2947C>A	NP_001361749.1:p.Pro983Thr
NM_001374828.1:c.2908C>A MANE Select	NP_001361757.1:p.Pro970Thr
NM_017519.3:c.2908C>A	NP_059989.3:p.Pro970Thr