Canonical Allele Identifier: CA571903935

Gene: ARID1B

Linked Data

• dbSNP Id: rs770700355
• gnomAD v2: 6-157510754-C-G
• gnomAD v4: 6-157189620-C-G
• MyVariant Identifiers: chr6:g.157510754C>G (hg19) ; chr6:g.157189620C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189620C>G , CM000668.2:g.157189620C>G	GRCh38
NC_000006.11:g.157510754C>G , CM000668.1:g.157510754C>G	GRCh37
NC_000006.10:g.157552446C>G	NCBI36
NG_032093.1:g.416691C>G
NG_032093.2:g.416691C>G
NG_066624.1:g.418595C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3761-22C>G	ENSP00000055163.8:n.3761-22C>G
ENST00000414678.8:c.3830-22C>G	ENSP00000412835.3:n.3830-22C>G
ENST00000637015.2:c.4049-22C>G	ENSP00000489729.2:n.4049-22C>G
ENST00000346085.10:c.3800-22C>G	ENSP00000344546.5:n.3800-22C>G
ENST00000350026.10:c.3512-22C>G	ENSP00000055163.7:n.3512-22C>G
ENST00000414678.7:c.2078-22C>G	ENSP00000412835.2:n.2078-22C>G
ENST00000635849.1:c.1241-22C>G	ENSP00000490948.1:n.1241-22C>G
ENST00000635957.1:c.875-22C>G	ENSP00000490385.1:n.875-22C>G
ENST00000636930.2:c.3920-22C>G MANE Select	ENSP00000490491.2:n.3920-22C>G
ENST00000636940.1:n.1917-22C>G
ENST00000637015.1:c.1288-22C>G
ENST00000637568.1:c.1202-22C>G
ENST00000637741.1:n.586-22C>G
ENST00000637810.1:c.1262-22C>G	ENSP00000489636.1:n.1262-22C>G
ENST00000637904.1:c.1421-22C>G	ENSP00000490550.1:n.1421-22C>G
ENST00000647938.1:c.3551-22C>G	ENSP00000498155.1:n.3551-22C>G
ENST00000346085.9:c.3551-22C>G	ENSP00000344546.4:n.3551-22C>G
ENST00000350026.9:c.3512-22C>G	ENSP00000055163.7:n.3512-22C>G
ENST00000414678.6:c.2078-22C>G	ENSP00000412835.2:n.2078-22C>G
NM_017519.2:c.3512-22C>G	NP_059989.2:n.3512-22C>G
NM_020732.3:c.3551-22C>G	NP_065783.3:n.3551-22C>G
XM_005267069.3:c.3671-22C>G	XP_005267126.2:n.3671-22C>G
XM_011535984.1:c.2750-22C>G	XP_011534286.1:n.2750-22C>G
XM_011535985.1:c.2570-22C>G	XP_011534287.1:n.2570-22C>G
XM_011535986.1:c.2330-22C>G	XP_011534288.1:n.2330-22C>G
XM_011535987.1:c.1949-22C>G	XP_011534289.1:n.1949-22C>G
XM_011535988.1:c.812-22C>G	XP_011534290.1:n.812-22C>G
NM_001346813.1:c.3671-22C>G	NP_001333742.1:n.3671-22C>G
NM_001363725.1:c.1421-22C>G	NP_001350654.1:n.1421-22C>G
XM_011535984.2:c.3881-22C>G	XP_011534286.2:n.3881-22C>G
XM_011535988.3:c.812-22C>G	XP_011534290.1:n.812-22C>G
XM_017011103.2:c.3782-22C>G	XP_016866592.1:n.3782-22C>G
XM_017011104.1:c.3752-22C>G	XP_016866593.1:n.3752-22C>G
XM_017011105.2:c.3722-22C>G	XP_016866594.1:n.3722-22C>G
XM_017011106.2:c.3593-22C>G	XP_016866595.1:n.3593-22C>G
XM_017011107.2:c.3572-22C>G	XP_016866596.1:n.3572-22C>G
XR_002956289.1:n.3964-22C>G
NM_001363725.2:c.1421-22C>G	NP_001350654.1:n.1421-22C>G
NM_001371656.1:c.3800-22C>G	NP_001358585.1:n.3800-22C>G
NM_001374820.1:c.3800-22C>G	NP_001361749.1:n.3800-22C>G
NM_001374828.1:c.3920-22C>G MANE Select	NP_001361757.1:n.3920-22C>G
NM_017519.3:c.3761-22C>G	NP_059989.3:n.3761-22C>G