Canonical Allele Identifier: CA366241934

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522224T>G (hg19) ; chr6:g.157201090T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201090T>G , CM000668.2:g.157201090T>G	GRCh38
NC_000006.11:g.157522224T>G , CM000668.1:g.157522224T>G	GRCh37
NC_000006.10:g.157563916T>G	NCBI36
NG_032093.1:g.428161T>G
NG_032093.2:g.428161T>G
NG_066624.1:g.430065T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4706T>G	ENSP00000055163.8:p.Met1569Arg
ENST00000414678.8:c.4775T>G	ENSP00000412835.3:p.Met1592Arg
ENST00000637015.2:c.4994T>G	ENSP00000489729.2:p.Met1665Arg
ENST00000346085.10:c.4745T>G	ENSP00000344546.5:p.Met1582Arg
ENST00000350026.10:c.4457T>G	ENSP00000055163.7:p.Met1486Arg
ENST00000414678.7:c.3023T>G	ENSP00000412835.2:p.Met1008Arg
ENST00000635849.1:c.2186T>G	ENSP00000490948.1:p.Met729Arg
ENST00000635957.1:c.1817T>G	ENSP00000490385.1:p.Met606Arg
ENST00000636227.1:n.3328T>G
ENST00000636254.1:n.785T>G
ENST00000636930.2:c.4865T>G MANE Select	ENSP00000490491.2:p.Met1622Arg
ENST00000636940.1:n.2862T>G
ENST00000637015.1:c.2233T>G
ENST00000637568.1:c.2147T>G
ENST00000637741.1:n.1531T>G
ENST00000637810.1:c.2207T>G	ENSP00000489636.1:p.Met736Arg
ENST00000637904.1:c.2366T>G	ENSP00000490550.1:p.Met789Arg
ENST00000647938.1:c.4496T>G	ENSP00000498155.1:p.Met1499Arg
ENST00000346085.9:c.4496T>G	ENSP00000344546.4:p.Met1499Arg
ENST00000350026.9:c.4457T>G	ENSP00000055163.7:p.Met1486Arg
ENST00000414678.6:c.3023T>G	ENSP00000412835.2:p.Met1008Arg
NM_017519.2:c.4457T>G	NP_059989.2:p.Met1486Arg
NM_020732.3:c.4496T>G	NP_065783.3:p.Met1499Arg
XM_005267069.3:c.4616T>G	XP_005267126.2:p.Met1539Arg
XM_011535984.1:c.3695T>G	XP_011534286.1:p.Met1232Arg
XM_011535985.1:c.3515T>G	XP_011534287.1:p.Met1172Arg
XM_011535986.1:c.3275T>G	XP_011534288.1:p.Met1092Arg
XM_011535987.1:c.2894T>G	XP_011534289.1:p.Met965Arg
XM_011535988.1:c.1757T>G	XP_011534290.1:p.Met586Arg
NM_001346813.1:c.4616T>G	NP_001333742.1:p.Met1539Arg
NM_001363725.1:c.2366T>G	NP_001350654.1:p.Met789Arg
XM_011535984.2:c.4826T>G	XP_011534286.2:p.Met1609Arg
XM_011535988.3:c.1757T>G	XP_011534290.1:p.Met586Arg
XM_017011103.2:c.4727T>G	XP_016866592.1:p.Met1576Arg
XM_017011104.1:c.4697T>G	XP_016866593.1:p.Met1566Arg
XM_017011105.2:c.4667T>G	XP_016866594.1:p.Met1556Arg
XM_017011106.2:c.4538T>G	XP_016866595.1:p.Met1513Arg
XM_017011107.2:c.4517T>G	XP_016866596.1:p.Met1506Arg
XR_002956289.1:n.4812T>G
NM_001363725.2:c.2366T>G	NP_001350654.1:p.Met789Arg
NM_001371656.1:c.4745T>G	NP_001358585.1:p.Met1582Arg
NM_001374820.1:c.4745T>G	NP_001361749.1:p.Met1582Arg
NM_001374828.1:c.4865T>G MANE Select	NP_001361757.1:p.Met1622Arg
NM_017519.3:c.4706T>G	NP_059989.3:p.Met1569Arg