Canonical Allele Identifier: CA366234097

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510826A>G (hg19) ; chr6:g.157189692A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189692A>G , CM000668.2:g.157189692A>G	GRCh38
NC_000006.11:g.157510826A>G , CM000668.1:g.157510826A>G	GRCh37
NC_000006.10:g.157552518A>G	NCBI36
NG_032093.1:g.416763A>G
NG_032093.2:g.416763A>G
NG_066624.1:g.418667A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3811A>G	ENSP00000055163.8:p.Asn1271Asp
ENST00000414678.8:c.3880A>G	ENSP00000412835.3:p.Asn1294Asp
ENST00000637015.2:c.4099A>G	ENSP00000489729.2:p.Asn1367Asp
ENST00000346085.10:c.3850A>G	ENSP00000344546.5:p.Asn1284Asp
ENST00000350026.10:c.3562A>G	ENSP00000055163.7:p.Asn1188Asp
ENST00000414678.7:c.2128A>G	ENSP00000412835.2:p.Asn710Asp
ENST00000635849.1:c.1291A>G	ENSP00000490948.1:p.Asn431Asp
ENST00000635957.1:c.925A>G	ENSP00000490385.1:p.Asn309Asp
ENST00000636930.2:c.3970A>G MANE Select	ENSP00000490491.2:p.Asn1324Asp
ENST00000636940.1:n.1967A>G
ENST00000637015.1:c.1338A>G
ENST00000637568.1:c.1252A>G
ENST00000637741.1:n.636A>G
ENST00000637810.1:c.1312A>G	ENSP00000489636.1:p.Asn438Asp
ENST00000637904.1:c.1471A>G	ENSP00000490550.1:p.Asn491Asp
ENST00000647938.1:c.3601A>G	ENSP00000498155.1:p.Asn1201Asp
ENST00000346085.9:c.3601A>G	ENSP00000344546.4:p.Asn1201Asp
ENST00000350026.9:c.3562A>G	ENSP00000055163.7:p.Asn1188Asp
ENST00000414678.6:c.2128A>G	ENSP00000412835.2:p.Asn710Asp
NM_017519.2:c.3562A>G	NP_059989.2:p.Asn1188Asp
NM_020732.3:c.3601A>G	NP_065783.3:p.Asn1201Asp
XM_005267069.3:c.3721A>G	XP_005267126.2:p.Asn1241Asp
XM_011535984.1:c.2800A>G	XP_011534286.1:p.Asn934Asp
XM_011535985.1:c.2620A>G	XP_011534287.1:p.Asn874Asp
XM_011535986.1:c.2380A>G	XP_011534288.1:p.Asn794Asp
XM_011535987.1:c.1999A>G	XP_011534289.1:p.Asn667Asp
XM_011535988.1:c.862A>G	XP_011534290.1:p.Asn288Asp
NM_001346813.1:c.3721A>G	NP_001333742.1:p.Asn1241Asp
NM_001363725.1:c.1471A>G	NP_001350654.1:p.Asn491Asp
XM_011535984.2:c.3931A>G	XP_011534286.2:p.Asn1311Asp
XM_011535988.3:c.862A>G	XP_011534290.1:p.Asn288Asp
XM_017011103.2:c.3832A>G	XP_016866592.1:p.Asn1278Asp
XM_017011104.1:c.3802A>G	XP_016866593.1:p.Asn1268Asp
XM_017011105.2:c.3772A>G	XP_016866594.1:p.Asn1258Asp
XM_017011106.2:c.3643A>G	XP_016866595.1:p.Asn1215Asp
XM_017011107.2:c.3622A>G	XP_016866596.1:p.Asn1208Asp
XR_002956289.1:n.4014A>G
NM_001363725.2:c.1471A>G	NP_001350654.1:p.Asn491Asp
NM_001371656.1:c.3850A>G	NP_001358585.1:p.Asn1284Asp
NM_001374820.1:c.3850A>G	NP_001361749.1:p.Asn1284Asp
NM_001374828.1:c.3970A>G MANE Select	NP_001361757.1:p.Asn1324Asp
NM_017519.3:c.3811A>G	NP_059989.3:p.Asn1271Asp