Canonical Allele Identifier: CA1096265107

Gene: ARID1B

Linked Data

• dbSNP Id: rs1788940772
• gnomAD v3: 6-156901540-CTG-C
• gnomAD v4: 6-156901540-CTG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156901541_156901542del , CM000668.2:g.156901541_156901542del	GRCh38
NC_000006.11:g.157222675_157222676del , CM000668.1:g.157222675_157222676del	GRCh37
NC_000006.10:g.157264367_157264368del	NCBI36
NG_032093.1:g.128612_128613del
NG_032093.2:g.128612_128613del
NG_066624.1:g.130516_130517del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2136+16_2136+17del	ENSP00000055163.8:n.2136+16_2136+17del
ENST00000414678.8:c.2136+16_2136+17del	ENSP00000412835.3:n.2136+16_2136+17del
ENST00000637015.2:c.2136+16_2136+17del	ENSP00000489729.2:n.2136+16_2136+17del
ENST00000319584.11:c.150+16_150+17del	ENSP00000313006.7:n.150+16_150+17del
ENST00000346085.10:c.2175+16_2175+17del	ENSP00000344546.5:n.2175+16_2175+17del
ENST00000350026.10:c.1887+16_1887+17del	ENSP00000055163.7:n.1887+16_1887+17del
ENST00000414678.7:c.384+16_384+17del	ENSP00000412835.2:n.384+16_384+17del
ENST00000636205.1:n.215_216del
ENST00000636748.1:c.417+16_417+17del	ENSP00000489917.1:n.417+16_417+17del
ENST00000636930.2:c.2136+16_2136+17del MANE Select	ENSP00000490491.2:n.2136+16_2136+17del
ENST00000637532.1:c.162+16_162+17del	ENSP00000490420.1:n.162+16_162+17del
ENST00000638000.1:c.353+16_353+17del
ENST00000647938.1:c.1926+16_1926+17del	ENSP00000498155.1:n.1926+16_1926+17del
ENST00000674190.1:n.843+16_843+17del
ENST00000674298.1:c.1876+16_1876+17del
ENST00000319584.10:c.153+16_153+17del	ENSP00000313006.6:n.153+16_153+17del
ENST00000346085.9:c.1926+16_1926+17del	ENSP00000344546.4:n.1926+16_1926+17del
ENST00000350026.9:c.1887+16_1887+17del	ENSP00000055163.7:n.1887+16_1887+17del
ENST00000414678.6:c.384+16_384+17del	ENSP00000412835.2:n.384+16_384+17del
NM_017519.2:c.1887+16_1887+17del	NP_059989.2:n.1887+16_1887+17del
NM_020732.3:c.1926+16_1926+17del	NP_065783.3:n.1926+16_1926+17del
XM_005267069.3:c.1887+16_1887+17del	XP_005267126.2:n.1887+16_1887+17del
XM_011535984.1:c.795+16_795+17del	XP_011534286.1:n.795+16_795+17del
XM_011535985.1:c.795+16_795+17del	XP_011534287.1:n.795+16_795+17del
XM_011535986.1:c.375+16_375+17del	XP_011534288.1:n.375+16_375+17del
NM_001346813.1:c.1887+16_1887+17del	NP_001333742.1:n.1887+16_1887+17del
XM_011535984.2:c.1926+16_1926+17del	XP_011534286.2:n.1926+16_1926+17del
XM_017011103.2:c.1926+16_1926+17del	XP_016866592.1:n.1926+16_1926+17del
XM_017011104.1:c.1926+16_1926+17del	XP_016866593.1:n.1926+16_1926+17del
XM_017011105.2:c.1926+16_1926+17del	XP_016866594.1:n.1926+16_1926+17del
XM_017011106.2:c.1926+16_1926+17del	XP_016866595.1:n.1926+16_1926+17del
XM_017011107.2:c.1926+16_1926+17del	XP_016866596.1:n.1926+16_1926+17del
XR_002956289.1:n.2009+16_2009+17del
NM_001371656.1:c.2175+16_2175+17del	NP_001358585.1:n.2175+16_2175+17del
NM_001374820.1:c.2175+16_2175+17del	NP_001361749.1:n.2175+16_2175+17del
NM_001374828.1:c.2136+16_2136+17del MANE Select	NP_001361757.1:n.2136+16_2136+17del
NM_017519.3:c.2136+16_2136+17del	NP_059989.3:n.2136+16_2136+17del