Canonical Allele Identifier: CA2713413854

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128339384

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189949_157189963del , CM000668.2:g.157189949_157189963del	GRCh38
NC_000006.11:g.157511083_157511097del , CM000668.1:g.157511083_157511097del	GRCh37
NC_000006.10:g.157552775_157552789del	NCBI36
NG_032093.1:g.417020_417034del
NG_032093.2:g.417020_417034del
NG_066624.1:g.418924_418938del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3900-89_3900-75del	ENSP00000055163.8:n.3900-89_3900-75del
ENST00000414678.8:c.3969-89_3969-75del	ENSP00000412835.3:n.3969-89_3969-75del
ENST00000637015.2:c.4188-89_4188-75del	ENSP00000489729.2:n.4188-89_4188-75del
ENST00000346085.10:c.3939-89_3939-75del	ENSP00000344546.5:n.3939-89_3939-75del
ENST00000350026.10:c.3651-89_3651-75del	ENSP00000055163.7:n.3651-89_3651-75del
ENST00000414678.7:c.2217-89_2217-75del	ENSP00000412835.2:n.2217-89_2217-75del
ENST00000635849.1:c.1380-89_1380-75del	ENSP00000490948.1:n.1380-89_1380-75del
ENST00000635957.1:c.1014-92_1014-78del	ENSP00000490385.1:n.1014-92_1014-78del
ENST00000636930.2:c.4059-89_4059-75del MANE Select	ENSP00000490491.2:n.4059-89_4059-75del
ENST00000636940.1:n.2056-89_2056-75del
ENST00000637015.1:c.1427-89_1427-75del
ENST00000637568.1:c.1341-89_1341-75del
ENST00000637741.1:n.725-89_725-75del
ENST00000637810.1:c.1401-89_1401-75del	ENSP00000489636.1:n.1401-89_1401-75del
ENST00000637904.1:c.1560-89_1560-75del	ENSP00000490550.1:n.1560-89_1560-75del
ENST00000647938.1:c.3690-89_3690-75del	ENSP00000498155.1:n.3690-89_3690-75del
ENST00000346085.9:c.3690-89_3690-75del	ENSP00000344546.4:n.3690-89_3690-75del
ENST00000350026.9:c.3651-89_3651-75del	ENSP00000055163.7:n.3651-89_3651-75del
ENST00000414678.6:c.2217-89_2217-75del	ENSP00000412835.2:n.2217-89_2217-75del
NM_017519.2:c.3651-89_3651-75del	NP_059989.2:n.3651-89_3651-75del
NM_020732.3:c.3690-89_3690-75del	NP_065783.3:n.3690-89_3690-75del
XM_005267069.3:c.3810-89_3810-75del	XP_005267126.2:n.3810-89_3810-75del
XM_011535984.1:c.2889-89_2889-75del	XP_011534286.1:n.2889-89_2889-75del
XM_011535985.1:c.2709-89_2709-75del	XP_011534287.1:n.2709-89_2709-75del
XM_011535986.1:c.2469-89_2469-75del	XP_011534288.1:n.2469-89_2469-75del
XM_011535987.1:c.2088-89_2088-75del	XP_011534289.1:n.2088-89_2088-75del
XM_011535988.1:c.951-89_951-75del	XP_011534290.1:n.951-89_951-75del
NM_001346813.1:c.3810-89_3810-75del	NP_001333742.1:n.3810-89_3810-75del
NM_001363725.1:c.1560-89_1560-75del	NP_001350654.1:n.1560-89_1560-75del
XM_011535984.2:c.4020-89_4020-75del	XP_011534286.2:n.4020-89_4020-75del
XM_011535988.3:c.951-89_951-75del	XP_011534290.1:n.951-89_951-75del
XM_017011103.2:c.3921-89_3921-75del	XP_016866592.1:n.3921-89_3921-75del
XM_017011104.1:c.3891-89_3891-75del	XP_016866593.1:n.3891-89_3891-75del
XM_017011105.2:c.3861-89_3861-75del	XP_016866594.1:n.3861-89_3861-75del
XM_017011106.2:c.3732-89_3732-75del	XP_016866595.1:n.3732-89_3732-75del
XM_017011107.2:c.3711-89_3711-75del	XP_016866596.1:n.3711-89_3711-75del
XR_002956289.1:n.4103-89_4103-75del
NM_001363725.2:c.1560-89_1560-75del	NP_001350654.1:n.1560-89_1560-75del
NM_001371656.1:c.3939-89_3939-75del	NP_001358585.1:n.3939-89_3939-75del
NM_001374820.1:c.3939-89_3939-75del	NP_001361749.1:n.3939-89_3939-75del
NM_001374828.1:c.4059-89_4059-75del MANE Select	NP_001361757.1:n.4059-89_4059-75del
NM_017519.3:c.3900-89_3900-75del	NP_059989.3:n.3900-89_3900-75del