Canonical Allele Identifier: CA366388602

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1527910
• ClinVar RCV Id: RCV002074476
• dbSNP Id: rs2128633891
• gnomAD v4: 6-157148624-G-T
• MyVariant Identifiers: chr6:g.157469758G>T (hg19) ; chr6:g.157148624G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148624G>T , CM000668.2:g.157148624G>T	GRCh38
NC_000006.11:g.157469758G>T , CM000668.1:g.157469758G>T	GRCh37
NC_000006.10:g.157511450G>T	NCBI36
NG_032093.1:g.375695G>T
NG_032093.2:g.375695G>T
NG_066624.1:g.377599G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2762G>T	ENSP00000055163.8:p.Gly921Val
ENST00000414678.8:c.2672G>T	ENSP00000412835.3:p.Gly891Val
ENST00000637015.2:c.2762G>T	ENSP00000489729.2:p.Gly921Val
ENST00000319584.11:c.776G>T	ENSP00000313006.7:p.Gly259Val
ENST00000346085.10:c.2801G>T	ENSP00000344546.5:p.Gly934Val
ENST00000350026.10:c.2513G>T	ENSP00000055163.7:p.Gly838Val
ENST00000414678.7:c.920G>T	ENSP00000412835.2:p.Gly307Val
ENST00000452544.2:n.663G>T
ENST00000635849.1:c.83G>T	ENSP00000490948.1:p.Gly28Val
ENST00000636930.2:c.2762G>T MANE Select	ENSP00000490491.2:p.Gly921Val
ENST00000637015.1:c.1G>T
ENST00000637810.1:c.263G>T	ENSP00000489636.1:p.Gly88Val
ENST00000637904.1:c.263G>T	ENSP00000490550.1:p.Gly88Val
ENST00000647938.1:c.2552G>T	ENSP00000498155.1:p.Gly851Val
ENST00000674190.1:n.1511G>T
ENST00000319584.10:c.779G>T	ENSP00000313006.6:p.Gly260Val
ENST00000346085.9:c.2552G>T	ENSP00000344546.4:p.Gly851Val
ENST00000350026.9:c.2513G>T	ENSP00000055163.7:p.Gly838Val
ENST00000414678.6:c.920G>T	ENSP00000412835.2:p.Gly307Val
ENST00000452544.1:n.609G>T
NM_017519.2:c.2513G>T	NP_059989.2:p.Gly838Val
NM_020732.3:c.2552G>T	NP_065783.3:p.Gly851Val
XM_005267069.3:c.2513G>T	XP_005267126.2:p.Gly838Val
XM_011535984.1:c.1463G>T	XP_011534286.1:p.Gly488Val
XM_011535985.1:c.1283G>T	XP_011534287.1:p.Gly428Val
XM_011535986.1:c.1043G>T	XP_011534288.1:p.Gly348Val
XM_011535987.1:c.662G>T	XP_011534289.1:p.Gly221Val
XM_011535988.1:c.-20+15417G>T	XP_011534290.1:n.-20+15417G>T
NM_001346813.1:c.2513G>T	NP_001333742.1:p.Gly838Val
NM_001363725.1:c.263G>T	NP_001350654.1:p.Gly88Val
XM_011535984.2:c.2594G>T	XP_011534286.2:p.Gly865Val
XM_011535988.3:c.-20+15417G>T	XP_011534290.1:n.-20+15417G>T
XM_017011103.2:c.2594G>T	XP_016866592.1:p.Gly865Val
XM_017011104.1:c.2594G>T	XP_016866593.1:p.Gly865Val
XM_017011105.2:c.2594G>T	XP_016866594.1:p.Gly865Val
XM_017011106.2:c.2594G>T	XP_016866595.1:p.Gly865Val
XM_017011107.2:c.2414G>T	XP_016866596.1:p.Gly805Val
XR_002956289.1:n.2677G>T
NM_001363725.2:c.263G>T	NP_001350654.1:p.Gly88Val
NM_001371656.1:c.2801G>T	NP_001358585.1:p.Gly934Val
NM_001374820.1:c.2801G>T	NP_001361749.1:p.Gly934Val
NM_001374828.1:c.2762G>T MANE Select	NP_001361757.1:p.Gly921Val
NM_017519.3:c.2762G>T	NP_059989.3:p.Gly921Val