Canonical Allele Identifier: CA150362430

Gene: ARID1B

Linked Data

• dbSNP Id: rs898828558
• gnomAD v2: 6-157510502-T-TCTTTTGACC
• gnomAD v3: 6-157189368-T-TCTTTTGACC
• gnomAD v4: 6-157189368-T-TCTTTTGACC
• MyVariant Identifiers: chr6:g.157510502_157510503insCTTTTGACC (hg19) ; chr6:g.157189368_157189369insCTTTTGACC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189369_157189370insTTTTGACCC , CM000668.2:g.157189369_157189370insTTTTGACCC	GRCh38
NC_000006.11:g.157510503_157510504insTTTTGACCC , CM000668.1:g.157510503_157510504insTTTTGACCC	GRCh37
NC_000006.10:g.157552195_157552196insTTTTGACCC	NCBI36
NG_032093.1:g.416440_416441insTTTTGACCC
NG_032093.2:g.416440_416441insTTTTGACCC
NG_066624.1:g.418344_418345insTTTTGACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3761-273_3761-272insTTTTGACCC	ENSP00000055163.8:n.3761-273_3761-272insTTTTGACCC
ENST00000414678.8:c.3830-273_3830-272insTTTTGACCC	ENSP00000412835.3:n.3830-273_3830-272insTTTTGACCC
ENST00000637015.2:c.4049-273_4049-272insTTTTGACCC	ENSP00000489729.2:n.4049-273_4049-272insTTTTGACCC
ENST00000346085.10:c.3800-273_3800-272insTTTTGACCC	ENSP00000344546.5:n.3800-273_3800-272insTTTTGACCC
ENST00000350026.10:c.3512-273_3512-272insTTTTGACCC	ENSP00000055163.7:n.3512-273_3512-272insTTTTGACCC
ENST00000414678.7:c.2078-273_2078-272insTTTTGACCC	ENSP00000412835.2:n.2078-273_2078-272insTTTTGACCC
ENST00000635849.1:c.1241-273_1241-272insTTTTGACCC	ENSP00000490948.1:n.1241-273_1241-272insTTTTGACCC
ENST00000635957.1:c.875-273_875-272insTTTTGACCC	ENSP00000490385.1:n.875-273_875-272insTTTTGACCC
ENST00000636930.2:c.3920-273_3920-272insTTTTGACCC MANE Select	ENSP00000490491.2:n.3920-273_3920-272insTTTTGACCC
ENST00000636940.1:n.1917-273_1917-272insTTTTGACCC
ENST00000637015.1:c.1288-273_1288-272insTTTTGACCC
ENST00000637568.1:c.1202-273_1202-272insTTTTGACCC
ENST00000637741.1:n.586-273_586-272insTTTTGACCC
ENST00000637810.1:c.1262-273_1262-272insTTTTGACCC	ENSP00000489636.1:n.1262-273_1262-272insTTTTGACCC
ENST00000637904.1:c.1421-273_1421-272insTTTTGACCC	ENSP00000490550.1:n.1421-273_1421-272insTTTTGACCC
ENST00000647938.1:c.3551-273_3551-272insTTTTGACCC	ENSP00000498155.1:n.3551-273_3551-272insTTTTGACCC
ENST00000346085.9:c.3551-273_3551-272insTTTTGACCC	ENSP00000344546.4:n.3551-273_3551-272insTTTTGACCC
ENST00000350026.9:c.3512-273_3512-272insTTTTGACCC	ENSP00000055163.7:n.3512-273_3512-272insTTTTGACCC
ENST00000414678.6:c.2078-273_2078-272insTTTTGACCC	ENSP00000412835.2:n.2078-273_2078-272insTTTTGACCC
NM_017519.2:c.3512-273_3512-272insTTTTGACCC	NP_059989.2:n.3512-273_3512-272insTTTTGACCC
NM_020732.3:c.3551-273_3551-272insTTTTGACCC	NP_065783.3:n.3551-273_3551-272insTTTTGACCC
XM_005267069.3:c.3671-273_3671-272insTTTTGACCC	XP_005267126.2:n.3671-273_3671-272insTTTTGACCC
XM_011535984.1:c.2750-273_2750-272insTTTTGACCC	XP_011534286.1:n.2750-273_2750-272insTTTTGACCC
XM_011535985.1:c.2570-273_2570-272insTTTTGACCC	XP_011534287.1:n.2570-273_2570-272insTTTTGACCC
XM_011535986.1:c.2330-273_2330-272insTTTTGACCC	XP_011534288.1:n.2330-273_2330-272insTTTTGACCC
XM_011535987.1:c.1949-273_1949-272insTTTTGACCC	XP_011534289.1:n.1949-273_1949-272insTTTTGACCC
XM_011535988.1:c.812-273_812-272insTTTTGACCC	XP_011534290.1:n.812-273_812-272insTTTTGACCC
NM_001346813.1:c.3671-273_3671-272insTTTTGACCC	NP_001333742.1:n.3671-273_3671-272insTTTTGACCC
NM_001363725.1:c.1421-273_1421-272insTTTTGACCC	NP_001350654.1:n.1421-273_1421-272insTTTTGACCC
XM_011535984.2:c.3881-273_3881-272insTTTTGACCC	XP_011534286.2:n.3881-273_3881-272insTTTTGACCC
XM_011535988.3:c.812-273_812-272insTTTTGACCC	XP_011534290.1:n.812-273_812-272insTTTTGACCC
XM_017011103.2:c.3782-273_3782-272insTTTTGACCC	XP_016866592.1:n.3782-273_3782-272insTTTTGACCC
XM_017011104.1:c.3752-273_3752-272insTTTTGACCC	XP_016866593.1:n.3752-273_3752-272insTTTTGACCC
XM_017011105.2:c.3722-273_3722-272insTTTTGACCC	XP_016866594.1:n.3722-273_3722-272insTTTTGACCC
XM_017011106.2:c.3593-273_3593-272insTTTTGACCC	XP_016866595.1:n.3593-273_3593-272insTTTTGACCC
XM_017011107.2:c.3572-273_3572-272insTTTTGACCC	XP_016866596.1:n.3572-273_3572-272insTTTTGACCC
XR_002956289.1:n.3964-273_3964-272insTTTTGACCC
NM_001363725.2:c.1421-273_1421-272insTTTTGACCC	NP_001350654.1:n.1421-273_1421-272insTTTTGACCC
NM_001371656.1:c.3800-273_3800-272insTTTTGACCC	NP_001358585.1:n.3800-273_3800-272insTTTTGACCC
NM_001374820.1:c.3800-273_3800-272insTTTTGACCC	NP_001361749.1:n.3800-273_3800-272insTTTTGACCC
NM_001374828.1:c.3920-273_3920-272insTTTTGACCC MANE Select	NP_001361757.1:n.3920-273_3920-272insTTTTGACCC
NM_017519.3:c.3761-273_3761-272insTTTTGACCC	NP_059989.3:n.3761-273_3761-272insTTTTGACCC