Canonical Allele Identifier: CA151044

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 126322
• ClinVar RCV Id: RCV000114265 ; RCV002433600 ; RCV002055272
• dbSNP Id: rs587779742
• ExAC: 6:157470005 G / A
• gnomAD v2: 6-157470005-G-A
• gnomAD v3: 6-157148871-G-A
• gnomAD v4: 6-157148871-G-A
• MyVariant Identifiers: chr6:g.157470005G>A (hg19) ; chr6:g.157148871G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148871G>A , CM000668.2:g.157148871G>A	GRCh38
NC_000006.11:g.157470005G>A , CM000668.1:g.157470005G>A	GRCh37
NC_000006.10:g.157511697G>A	NCBI36
NG_032093.1:g.375942G>A
NG_032093.2:g.375942G>A
NG_066624.1:g.377846G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3009G>A	ENSP00000055163.8:p.Pro1003=
ENST00000414678.8:c.2919G>A	ENSP00000412835.3:p.Pro973=
ENST00000637015.2:c.3009G>A	ENSP00000489729.2:p.Pro1003=
ENST00000319584.11:c.1023G>A	ENSP00000313006.7:p.Pro341=
ENST00000346085.10:c.3048G>A	ENSP00000344546.5:p.Pro1016=
ENST00000350026.10:c.2760G>A	ENSP00000055163.7:p.Pro920=
ENST00000414678.7:c.1167G>A	ENSP00000412835.2:p.Pro389=
ENST00000452544.2:n.910G>A
ENST00000635849.1:c.330G>A	ENSP00000490948.1:p.Pro110=
ENST00000636426.1:n.143G>A
ENST00000636930.2:c.3009G>A MANE Select	ENSP00000490491.2:p.Pro1003=
ENST00000637015.1:c.248G>A
ENST00000637568.1:c.52G>A
ENST00000637810.1:c.510G>A	ENSP00000489636.1:p.Pro170=
ENST00000637904.1:c.510G>A	ENSP00000490550.1:p.Pro170=
ENST00000647938.1:c.2799G>A	ENSP00000498155.1:p.Pro933=
ENST00000674190.1:n.1758G>A
ENST00000319584.10:c.1026G>A	ENSP00000313006.6:p.Pro342=
ENST00000346085.9:c.2799G>A	ENSP00000344546.4:p.Pro933=
ENST00000350026.9:c.2760G>A	ENSP00000055163.7:p.Pro920=
ENST00000414678.6:c.1167G>A	ENSP00000412835.2:p.Pro389=
ENST00000452544.1:n.856G>A
ENST00000478761.3:c.82G>A
NM_017519.2:c.2760G>A	NP_059989.2:p.Pro920=
NM_020732.3:c.2799G>A	NP_065783.3:p.Pro933=
XM_005267069.3:c.2760G>A	XP_005267126.2:p.Pro920=
XM_011535984.1:c.1710G>A	XP_011534286.1:p.Pro570=
XM_011535985.1:c.1530G>A	XP_011534287.1:p.Pro510=
XM_011535986.1:c.1290G>A	XP_011534288.1:p.Pro430=
XM_011535987.1:c.909G>A	XP_011534289.1:p.Pro303=
XM_011535988.1:c.-20+15664G>A	XP_011534290.1:n.-20+15664G>A
NM_001346813.1:c.2760G>A	NP_001333742.1:p.Pro920=
NM_001363725.1:c.510G>A	NP_001350654.1:p.Pro170=
XM_011535984.2:c.2841G>A	XP_011534286.2:p.Pro947=
XM_011535988.3:c.-20+15664G>A	XP_011534290.1:n.-20+15664G>A
XM_017011103.2:c.2841G>A	XP_016866592.1:p.Pro947=
XM_017011104.1:c.2841G>A	XP_016866593.1:p.Pro947=
XM_017011105.2:c.2841G>A	XP_016866594.1:p.Pro947=
XM_017011106.2:c.2841G>A	XP_016866595.1:p.Pro947=
XM_017011107.2:c.2661G>A	XP_016866596.1:p.Pro887=
XR_002956289.1:n.2924G>A
NM_001363725.2:c.510G>A	NP_001350654.1:p.Pro170=
NM_001371656.1:c.3048G>A	NP_001358585.1:p.Pro1016=
NM_001374820.1:c.3048G>A	NP_001361749.1:p.Pro1016=
NM_001374828.1:c.3009G>A MANE Select	NP_001361757.1:p.Pro1003=
NM_017519.3:c.3009G>A	NP_059989.3:p.Pro1003=