Canonical Allele Identifier: CA4067185

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1225348
• ClinVar RCV Id: RCV001610914
• dbSNP Id: rs777669434
• ExAC: 6:157470089 C / T
• gnomAD v2: 6-157470089-C-T
• gnomAD v3: 6-157148955-C-T
• gnomAD v4: 6-157148955-C-T
• MyVariant Identifiers: chr6:g.157470089C>T (hg19) ; chr6:g.157148955C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148955C>T , CM000668.2:g.157148955C>T	GRCh38
NC_000006.11:g.157470089C>T , CM000668.1:g.157470089C>T	GRCh37
NC_000006.10:g.157511781C>T	NCBI36
NG_032093.1:g.376026C>T
NG_032093.2:g.376026C>T
NG_066624.1:g.377930C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3089+4C>T	ENSP00000055163.8:n.3089+4C>T
ENST00000414678.8:c.2999+4C>T	ENSP00000412835.3:n.2999+4C>T
ENST00000637015.2:c.3089+4C>T	ENSP00000489729.2:n.3089+4C>T
ENST00000319584.11:c.1103+4C>T	ENSP00000313006.7:n.1103+4C>T
ENST00000346085.10:c.3128+4C>T	ENSP00000344546.5:n.3128+4C>T
ENST00000350026.10:c.2840+4C>T	ENSP00000055163.7:n.2840+4C>T
ENST00000414678.7:c.1247+4C>T	ENSP00000412835.2:n.1247+4C>T
ENST00000452544.2:n.994C>T
ENST00000635849.1:c.410+4C>T	ENSP00000490948.1:n.410+4C>T
ENST00000635957.1:c.44+4C>T	ENSP00000490385.1:n.44+4C>T
ENST00000636426.1:n.227C>T
ENST00000636930.2:c.3089+4C>T MANE Select	ENSP00000490491.2:n.3089+4C>T
ENST00000637015.1:c.328+4C>T
ENST00000637568.1:c.132+4C>T
ENST00000637810.1:c.590+4C>T	ENSP00000489636.1:n.590+4C>T
ENST00000637904.1:c.590+4C>T	ENSP00000490550.1:n.590+4C>T
ENST00000647938.1:c.2879+4C>T	ENSP00000498155.1:n.2879+4C>T
ENST00000674190.1:n.1838+4C>T
ENST00000319584.10:c.1106+4C>T	ENSP00000313006.6:n.1106+4C>T
ENST00000346085.9:c.2879+4C>T	ENSP00000344546.4:n.2879+4C>T
ENST00000350026.9:c.2840+4C>T	ENSP00000055163.7:n.2840+4C>T
ENST00000400790.3:c.41+4C>T	ENSP00000383596.3:n.41+4C>T
ENST00000414678.6:c.1247+4C>T	ENSP00000412835.2:n.1247+4C>T
ENST00000452544.1:n.940C>T
ENST00000478761.3:c.162+4C>T
NM_017519.2:c.2840+4C>T	NP_059989.2:n.2840+4C>T
NM_020732.3:c.2879+4C>T	NP_065783.3:n.2879+4C>T
XM_005267069.3:c.2840+4C>T	XP_005267126.2:n.2840+4C>T
XM_011535984.1:c.1790+4C>T	XP_011534286.1:n.1790+4C>T
XM_011535985.1:c.1610+4C>T	XP_011534287.1:n.1610+4C>T
XM_011535986.1:c.1370+4C>T	XP_011534288.1:n.1370+4C>T
XM_011535987.1:c.989+4C>T	XP_011534289.1:n.989+4C>T
XM_011535988.1:c.-20+15748C>T	XP_011534290.1:n.-20+15748C>T
NM_001346813.1:c.2840+4C>T	NP_001333742.1:n.2840+4C>T
NM_001363725.1:c.590+4C>T	NP_001350654.1:n.590+4C>T
XM_011535984.2:c.2921+4C>T	XP_011534286.2:n.2921+4C>T
XM_011535988.3:c.-20+15748C>T	XP_011534290.1:n.-20+15748C>T
XM_017011103.2:c.2925C>T	XP_016866592.1:p.Tyr975=
XM_017011104.1:c.2921+4C>T	XP_016866593.1:n.2921+4C>T
XM_017011105.2:c.2921+4C>T	XP_016866594.1:n.2921+4C>T
XM_017011106.2:c.2921+4C>T	XP_016866595.1:n.2921+4C>T
XM_017011107.2:c.2741+4C>T	XP_016866596.1:n.2741+4C>T
XR_002956289.1:n.3004+4C>T
NM_001363725.2:c.590+4C>T	NP_001350654.1:n.590+4C>T
NM_001371656.1:c.3128+4C>T	NP_001358585.1:n.3128+4C>T
NM_001374820.1:c.3128+4C>T	NP_001361749.1:n.3128+4C>T
NM_001374828.1:c.3089+4C>T MANE Select	NP_001361757.1:n.3089+4C>T
NM_017519.3:c.3089+4C>T	NP_059989.3:n.3089+4C>T