Canonical Allele Identifier: CA366242300

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522370A>G (hg19) ; chr6:g.157201236A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201236A>G , CM000668.2:g.157201236A>G	GRCh38
NC_000006.11:g.157522370A>G , CM000668.1:g.157522370A>G	GRCh37
NC_000006.10:g.157564062A>G	NCBI36
NG_032093.1:g.428307A>G
NG_032093.2:g.428307A>G
NG_066624.1:g.430211A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4852A>G	ENSP00000055163.8:p.Asn1618Asp
ENST00000414678.8:c.4921A>G	ENSP00000412835.3:p.Asn1641Asp
ENST00000637015.2:c.5140A>G	ENSP00000489729.2:p.Asn1714Asp
ENST00000346085.10:c.4891A>G	ENSP00000344546.5:p.Asn1631Asp
ENST00000350026.10:c.4603A>G	ENSP00000055163.7:p.Asn1535Asp
ENST00000414678.7:c.3169A>G	ENSP00000412835.2:p.Asn1057Asp
ENST00000635849.1:c.2332A>G	ENSP00000490948.1:p.Asn778Asp
ENST00000635957.1:c.1963A>G	ENSP00000490385.1:p.Asn655Asp
ENST00000636227.1:n.3474A>G
ENST00000636254.1:n.931A>G
ENST00000636930.2:c.5011A>G MANE Select	ENSP00000490491.2:p.Asn1671Asp
ENST00000636940.1:n.3008A>G
ENST00000637015.1:c.2379A>G
ENST00000637568.1:c.2293A>G
ENST00000637741.1:n.1677A>G
ENST00000637810.1:c.2353A>G	ENSP00000489636.1:p.Asn785Asp
ENST00000637904.1:c.2512A>G	ENSP00000490550.1:p.Asn838Asp
ENST00000647938.1:c.4642A>G	ENSP00000498155.1:p.Asn1548Asp
ENST00000346085.9:c.4642A>G	ENSP00000344546.4:p.Asn1548Asp
ENST00000350026.9:c.4603A>G	ENSP00000055163.7:p.Asn1535Asp
ENST00000414678.6:c.3169A>G	ENSP00000412835.2:p.Asn1057Asp
NM_017519.2:c.4603A>G	NP_059989.2:p.Asn1535Asp
NM_020732.3:c.4642A>G	NP_065783.3:p.Asn1548Asp
XM_005267069.3:c.4762A>G	XP_005267126.2:p.Asn1588Asp
XM_011535984.1:c.3841A>G	XP_011534286.1:p.Asn1281Asp
XM_011535985.1:c.3661A>G	XP_011534287.1:p.Asn1221Asp
XM_011535986.1:c.3421A>G	XP_011534288.1:p.Asn1141Asp
XM_011535987.1:c.3040A>G	XP_011534289.1:p.Asn1014Asp
XM_011535988.1:c.1903A>G	XP_011534290.1:p.Asn635Asp
NM_001346813.1:c.4762A>G	NP_001333742.1:p.Asn1588Asp
NM_001363725.1:c.2512A>G	NP_001350654.1:p.Asn838Asp
XM_011535984.2:c.4972A>G	XP_011534286.2:p.Asn1658Asp
XM_011535988.3:c.1903A>G	XP_011534290.1:p.Asn635Asp
XM_017011103.2:c.4873A>G	XP_016866592.1:p.Asn1625Asp
XM_017011104.1:c.4843A>G	XP_016866593.1:p.Asn1615Asp
XM_017011105.2:c.4813A>G	XP_016866594.1:p.Asn1605Asp
XM_017011106.2:c.4684A>G	XP_016866595.1:p.Asn1562Asp
XM_017011107.2:c.4663A>G	XP_016866596.1:p.Asn1555Asp
XR_002956289.1:n.4958A>G
NM_001363725.2:c.2512A>G	NP_001350654.1:p.Asn838Asp
NM_001371656.1:c.4891A>G	NP_001358585.1:p.Asn1631Asp
NM_001374820.1:c.4891A>G	NP_001361749.1:p.Asn1631Asp
NM_001374828.1:c.5011A>G MANE Select	NP_001361757.1:p.Asn1671Asp
NM_017519.3:c.4852A>G	NP_059989.3:p.Asn1618Asp