Canonical Allele Identifier: CA366235288

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511243T>G (hg19) ; chr6:g.157190109T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190109T>G , CM000668.2:g.157190109T>G	GRCh38
NC_000006.11:g.157511243T>G , CM000668.1:g.157511243T>G	GRCh37
NC_000006.10:g.157552935T>G	NCBI36
NG_032093.1:g.417180T>G
NG_032093.2:g.417180T>G
NG_066624.1:g.419084T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3971T>G	ENSP00000055163.8:p.Met1324Arg
ENST00000414678.8:c.4040T>G	ENSP00000412835.3:p.Met1347Arg
ENST00000637015.2:c.4259T>G	ENSP00000489729.2:p.Met1420Arg
ENST00000346085.10:c.4010T>G	ENSP00000344546.5:p.Met1337Arg
ENST00000350026.10:c.3722T>G	ENSP00000055163.7:p.Met1241Arg
ENST00000414678.7:c.2288T>G	ENSP00000412835.2:p.Met763Arg
ENST00000635849.1:c.1451T>G	ENSP00000490948.1:p.Met484Arg
ENST00000635957.1:c.1082T>G	ENSP00000490385.1:p.Met361Arg
ENST00000636930.2:c.4130T>G MANE Select	ENSP00000490491.2:p.Met1377Arg
ENST00000636940.1:n.2127T>G
ENST00000637015.1:c.1498T>G
ENST00000637568.1:c.1412T>G
ENST00000637741.1:n.796T>G
ENST00000637810.1:c.1472T>G	ENSP00000489636.1:p.Met491Arg
ENST00000637904.1:c.1631T>G	ENSP00000490550.1:p.Met544Arg
ENST00000647938.1:c.3761T>G	ENSP00000498155.1:p.Met1254Arg
ENST00000346085.9:c.3761T>G	ENSP00000344546.4:p.Met1254Arg
ENST00000350026.9:c.3722T>G	ENSP00000055163.7:p.Met1241Arg
ENST00000414678.6:c.2288T>G	ENSP00000412835.2:p.Met763Arg
NM_017519.2:c.3722T>G	NP_059989.2:p.Met1241Arg
NM_020732.3:c.3761T>G	NP_065783.3:p.Met1254Arg
XM_005267069.3:c.3881T>G	XP_005267126.2:p.Met1294Arg
XM_011535984.1:c.2960T>G	XP_011534286.1:p.Met987Arg
XM_011535985.1:c.2780T>G	XP_011534287.1:p.Met927Arg
XM_011535986.1:c.2540T>G	XP_011534288.1:p.Met847Arg
XM_011535987.1:c.2159T>G	XP_011534289.1:p.Met720Arg
XM_011535988.1:c.1022T>G	XP_011534290.1:p.Met341Arg
NM_001346813.1:c.3881T>G	NP_001333742.1:p.Met1294Arg
NM_001363725.1:c.1631T>G	NP_001350654.1:p.Met544Arg
XM_011535984.2:c.4091T>G	XP_011534286.2:p.Met1364Arg
XM_011535988.3:c.1022T>G	XP_011534290.1:p.Met341Arg
XM_017011103.2:c.3992T>G	XP_016866592.1:p.Met1331Arg
XM_017011104.1:c.3962T>G	XP_016866593.1:p.Met1321Arg
XM_017011105.2:c.3932T>G	XP_016866594.1:p.Met1311Arg
XM_017011106.2:c.3803T>G	XP_016866595.1:p.Met1268Arg
XM_017011107.2:c.3782T>G	XP_016866596.1:p.Met1261Arg
XR_002956289.1:n.4174T>G
NM_001363725.2:c.1631T>G	NP_001350654.1:p.Met544Arg
NM_001371656.1:c.4010T>G	NP_001358585.1:p.Met1337Arg
NM_001374820.1:c.4010T>G	NP_001361749.1:p.Met1337Arg
NM_001374828.1:c.4130T>G MANE Select	NP_001361757.1:p.Met1377Arg
NM_017519.3:c.3971T>G	NP_059989.3:p.Met1324Arg