Canonical Allele Identifier: CA1675538208

Gene: ARID1B

Linked Data

• dbSNP Id: rs1583479357
• gnomAD v4: 6-157189613-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189613C>T , CM000668.2:g.157189613C>T	GRCh38
NC_000006.11:g.157510747C>T , CM000668.1:g.157510747C>T	GRCh37
NC_000006.10:g.157552439C>T	NCBI36
NG_032093.1:g.416684C>T
NG_032093.2:g.416684C>T
NG_066624.1:g.418588C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3761-29C>T	ENSP00000055163.8:n.3761-29C>T
ENST00000414678.8:c.3830-29C>T	ENSP00000412835.3:n.3830-29C>T
ENST00000637015.2:c.4049-29C>T	ENSP00000489729.2:n.4049-29C>T
ENST00000346085.10:c.3800-29C>T	ENSP00000344546.5:n.3800-29C>T
ENST00000350026.10:c.3512-29C>T	ENSP00000055163.7:n.3512-29C>T
ENST00000414678.7:c.2078-29C>T	ENSP00000412835.2:n.2078-29C>T
ENST00000635849.1:c.1241-29C>T	ENSP00000490948.1:n.1241-29C>T
ENST00000635957.1:c.875-29C>T	ENSP00000490385.1:n.875-29C>T
ENST00000636930.2:c.3920-29C>T MANE Select	ENSP00000490491.2:n.3920-29C>T
ENST00000636940.1:n.1917-29C>T
ENST00000637015.1:c.1288-29C>T
ENST00000637568.1:c.1202-29C>T
ENST00000637741.1:n.586-29C>T
ENST00000637810.1:c.1262-29C>T	ENSP00000489636.1:n.1262-29C>T
ENST00000637904.1:c.1421-29C>T	ENSP00000490550.1:n.1421-29C>T
ENST00000647938.1:c.3551-29C>T	ENSP00000498155.1:n.3551-29C>T
ENST00000346085.9:c.3551-29C>T	ENSP00000344546.4:n.3551-29C>T
ENST00000350026.9:c.3512-29C>T	ENSP00000055163.7:n.3512-29C>T
ENST00000414678.6:c.2078-29C>T	ENSP00000412835.2:n.2078-29C>T
NM_017519.2:c.3512-29C>T	NP_059989.2:n.3512-29C>T
NM_020732.3:c.3551-29C>T	NP_065783.3:n.3551-29C>T
XM_005267069.3:c.3671-29C>T	XP_005267126.2:n.3671-29C>T
XM_011535984.1:c.2750-29C>T	XP_011534286.1:n.2750-29C>T
XM_011535985.1:c.2570-29C>T	XP_011534287.1:n.2570-29C>T
XM_011535986.1:c.2330-29C>T	XP_011534288.1:n.2330-29C>T
XM_011535987.1:c.1949-29C>T	XP_011534289.1:n.1949-29C>T
XM_011535988.1:c.812-29C>T	XP_011534290.1:n.812-29C>T
NM_001346813.1:c.3671-29C>T	NP_001333742.1:n.3671-29C>T
NM_001363725.1:c.1421-29C>T	NP_001350654.1:n.1421-29C>T
XM_011535984.2:c.3881-29C>T	XP_011534286.2:n.3881-29C>T
XM_011535988.3:c.812-29C>T	XP_011534290.1:n.812-29C>T
XM_017011103.2:c.3782-29C>T	XP_016866592.1:n.3782-29C>T
XM_017011104.1:c.3752-29C>T	XP_016866593.1:n.3752-29C>T
XM_017011105.2:c.3722-29C>T	XP_016866594.1:n.3722-29C>T
XM_017011106.2:c.3593-29C>T	XP_016866595.1:n.3593-29C>T
XM_017011107.2:c.3572-29C>T	XP_016866596.1:n.3572-29C>T
XR_002956289.1:n.3964-29C>T
NM_001363725.2:c.1421-29C>T	NP_001350654.1:n.1421-29C>T
NM_001371656.1:c.3800-29C>T	NP_001358585.1:n.3800-29C>T
NM_001374820.1:c.3800-29C>T	NP_001361749.1:n.3800-29C>T
NM_001374828.1:c.3920-29C>T MANE Select	NP_001361757.1:n.3920-29C>T
NM_017519.3:c.3761-29C>T	NP_059989.3:n.3761-29C>T