Canonical Allele Identifier: CA366234098

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3811A>T	ENSP00000055163.8:p.Asn1271Tyr
ENST00000414678.8:c.3880A>T	ENSP00000412835.3:p.Asn1294Tyr
ENST00000637015.2:c.4099A>T	ENSP00000489729.2:p.Asn1367Tyr
ENST00000346085.10:c.3850A>T	ENSP00000344546.5:p.Asn1284Tyr
ENST00000350026.10:c.3562A>T	ENSP00000055163.7:p.Asn1188Tyr
ENST00000414678.7:c.2128A>T	ENSP00000412835.2:p.Asn710Tyr
ENST00000635849.1:c.1291A>T	ENSP00000490948.1:p.Asn431Tyr
ENST00000635957.1:c.925A>T	ENSP00000490385.1:p.Asn309Tyr
ENST00000636930.2:c.3970A>T MANE Select	ENSP00000490491.2:p.Asn1324Tyr
ENST00000636940.1:n.1967A>T
ENST00000637015.1:c.1338A>T
ENST00000637568.1:c.1252A>T
ENST00000637741.1:n.636A>T
ENST00000637810.1:c.1312A>T	ENSP00000489636.1:p.Asn438Tyr
ENST00000637904.1:c.1471A>T	ENSP00000490550.1:p.Asn491Tyr
ENST00000647938.1:c.3601A>T	ENSP00000498155.1:p.Asn1201Tyr
ENST00000346085.9:c.3601A>T	ENSP00000344546.4:p.Asn1201Tyr
ENST00000350026.9:c.3562A>T	ENSP00000055163.7:p.Asn1188Tyr
ENST00000414678.6:c.2128A>T	ENSP00000412835.2:p.Asn710Tyr
NM_017519.2:c.3562A>T	NP_059989.2:p.Asn1188Tyr
NM_020732.3:c.3601A>T	NP_065783.3:p.Asn1201Tyr
XM_005267069.3:c.3721A>T	XP_005267126.2:p.Asn1241Tyr
XM_011535984.1:c.2800A>T	XP_011534286.1:p.Asn934Tyr
XM_011535985.1:c.2620A>T	XP_011534287.1:p.Asn874Tyr
XM_011535986.1:c.2380A>T	XP_011534288.1:p.Asn794Tyr
XM_011535987.1:c.1999A>T	XP_011534289.1:p.Asn667Tyr
XM_011535988.1:c.862A>T	XP_011534290.1:p.Asn288Tyr
NM_001346813.1:c.3721A>T	NP_001333742.1:p.Asn1241Tyr
NM_001363725.1:c.1471A>T	NP_001350654.1:p.Asn491Tyr
XM_011535984.2:c.3931A>T	XP_011534286.2:p.Asn1311Tyr
XM_011535988.3:c.862A>T	XP_011534290.1:p.Asn288Tyr
XM_017011103.2:c.3832A>T	XP_016866592.1:p.Asn1278Tyr
XM_017011104.1:c.3802A>T	XP_016866593.1:p.Asn1268Tyr
XM_017011105.2:c.3772A>T	XP_016866594.1:p.Asn1258Tyr
XM_017011106.2:c.3643A>T	XP_016866595.1:p.Asn1215Tyr
XM_017011107.2:c.3622A>T	XP_016866596.1:p.Asn1208Tyr
XR_002956289.1:n.4014A>T
NM_001363725.2:c.1471A>T	NP_001350654.1:p.Asn491Tyr
NM_001371656.1:c.3850A>T	NP_001358585.1:p.Asn1284Tyr
NM_001374820.1:c.3850A>T	NP_001361749.1:p.Asn1284Tyr
NM_001374828.1:c.3970A>T MANE Select	NP_001361757.1:p.Asn1324Tyr
NM_017519.3:c.3811A>T	NP_059989.3:p.Asn1271Tyr