Canonical Allele Identifier: CA151035

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 126316
• ClinVar RCV Id: RCV000114259 ; RCV001573077 ; RCV004542809 ; RCV001807043 ; RCV002312000
• dbSNP Id: rs17318151
• ExAC: 6:157150496 A / G
• gnomAD v2: 6-157150496-A-G
• gnomAD v3: 6-156829362-A-G
• gnomAD v4: 6-156829362-A-G
• MyVariant Identifiers: chr6:g.157150496A>G (hg19) ; chr6:g.156829362A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156829362A>G , CM000668.2:g.156829362A>G	GRCh38
NC_000006.11:g.157150496A>G , CM000668.1:g.157150496A>G	GRCh37
NC_000006.10:g.157192188A>G	NCBI36
NG_032093.1:g.56433A>G
NG_032093.2:g.56433A>G
NG_066624.1:g.58337A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.1927A>G	ENSP00000055163.8:p.Ile643Val
ENST00000414678.8:c.1927A>G	ENSP00000412835.3:p.Ile643Val
ENST00000637015.2:c.1927A>G	ENSP00000489729.2:p.Ile643Val
ENST00000346085.10:c.1927A>G	ENSP00000344546.5:p.Ile643Val
ENST00000350026.10:c.1678A>G	ENSP00000055163.7:p.Ile560Val
ENST00000414678.7:c.175A>G	ENSP00000412835.2:p.Ile59Val
ENST00000494260.2:c.208A>G	ENSP00000490094.1:p.Ile70Val
ENST00000636607.1:c.190A>G	ENSP00000490050.1:p.Ile64Val
ENST00000636748.1:c.208A>G	ENSP00000489917.1:p.Ile70Val
ENST00000636930.2:c.1927A>G MANE Select	ENSP00000490491.2:p.Ile643Val
ENST00000637910.1:n.208A>G
ENST00000638000.1:c.144A>G
ENST00000647938.1:c.1678A>G	ENSP00000498155.1:p.Ile560Val
ENST00000674190.1:n.634A>G
ENST00000674298.1:c.1667A>G
ENST00000346085.9:c.1678A>G	ENSP00000344546.4:p.Ile560Val
ENST00000350026.9:c.1678A>G	ENSP00000055163.7:p.Ile560Val
ENST00000414678.6:c.175A>G	ENSP00000412835.2:p.Ile59Val
ENST00000494260.1:n.136A>G
NM_017519.2:c.1678A>G	NP_059989.2:p.Ile560Val
NM_020732.3:c.1678A>G	NP_065783.3:p.Ile560Val
XM_005267069.3:c.1678A>G	XP_005267126.2:p.Ile560Val
XM_011535984.1:c.547A>G	XP_011534286.1:p.Ile183Val
XM_011535985.1:c.547A>G	XP_011534287.1:p.Ile183Val
XM_011535986.1:c.127A>G	XP_011534288.1:p.Ile43Val
NM_001346813.1:c.1678A>G	NP_001333742.1:p.Ile560Val
XM_011535984.2:c.1678A>G	XP_011534286.2:p.Ile560Val
XM_017011103.2:c.1678A>G	XP_016866592.1:p.Ile560Val
XM_017011104.1:c.1678A>G	XP_016866593.1:p.Ile560Val
XM_017011105.2:c.1678A>G	XP_016866594.1:p.Ile560Val
XM_017011106.2:c.1678A>G	XP_016866595.1:p.Ile560Val
XM_017011107.2:c.1678A>G	XP_016866596.1:p.Ile560Val
XR_002956289.1:n.1761A>G
NM_001371656.1:c.1927A>G	NP_001358585.1:p.Ile643Val
NM_001374820.1:c.1927A>G	NP_001361749.1:p.Ile643Val
NM_001374828.1:c.1927A>G MANE Select	NP_001361757.1:p.Ile643Val
NM_017519.3:c.1927A>G	NP_059989.3:p.Ile643Val