Canonical Allele Identifier: CA366235287

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3971T>A	ENSP00000055163.8:p.Met1324Lys
ENST00000414678.8:c.4040T>A	ENSP00000412835.3:p.Met1347Lys
ENST00000637015.2:c.4259T>A	ENSP00000489729.2:p.Met1420Lys
ENST00000346085.10:c.4010T>A	ENSP00000344546.5:p.Met1337Lys
ENST00000350026.10:c.3722T>A	ENSP00000055163.7:p.Met1241Lys
ENST00000414678.7:c.2288T>A	ENSP00000412835.2:p.Met763Lys
ENST00000635849.1:c.1451T>A	ENSP00000490948.1:p.Met484Lys
ENST00000635957.1:c.1082T>A	ENSP00000490385.1:p.Met361Lys
ENST00000636930.2:c.4130T>A MANE Select	ENSP00000490491.2:p.Met1377Lys
ENST00000636940.1:n.2127T>A
ENST00000637015.1:c.1498T>A
ENST00000637568.1:c.1412T>A
ENST00000637741.1:n.796T>A
ENST00000637810.1:c.1472T>A	ENSP00000489636.1:p.Met491Lys
ENST00000637904.1:c.1631T>A	ENSP00000490550.1:p.Met544Lys
ENST00000647938.1:c.3761T>A	ENSP00000498155.1:p.Met1254Lys
ENST00000346085.9:c.3761T>A	ENSP00000344546.4:p.Met1254Lys
ENST00000350026.9:c.3722T>A	ENSP00000055163.7:p.Met1241Lys
ENST00000414678.6:c.2288T>A	ENSP00000412835.2:p.Met763Lys
NM_017519.2:c.3722T>A	NP_059989.2:p.Met1241Lys
NM_020732.3:c.3761T>A	NP_065783.3:p.Met1254Lys
XM_005267069.3:c.3881T>A	XP_005267126.2:p.Met1294Lys
XM_011535984.1:c.2960T>A	XP_011534286.1:p.Met987Lys
XM_011535985.1:c.2780T>A	XP_011534287.1:p.Met927Lys
XM_011535986.1:c.2540T>A	XP_011534288.1:p.Met847Lys
XM_011535987.1:c.2159T>A	XP_011534289.1:p.Met720Lys
XM_011535988.1:c.1022T>A	XP_011534290.1:p.Met341Lys
NM_001346813.1:c.3881T>A	NP_001333742.1:p.Met1294Lys
NM_001363725.1:c.1631T>A	NP_001350654.1:p.Met544Lys
XM_011535984.2:c.4091T>A	XP_011534286.2:p.Met1364Lys
XM_011535988.3:c.1022T>A	XP_011534290.1:p.Met341Lys
XM_017011103.2:c.3992T>A	XP_016866592.1:p.Met1331Lys
XM_017011104.1:c.3962T>A	XP_016866593.1:p.Met1321Lys
XM_017011105.2:c.3932T>A	XP_016866594.1:p.Met1311Lys
XM_017011106.2:c.3803T>A	XP_016866595.1:p.Met1268Lys
XM_017011107.2:c.3782T>A	XP_016866596.1:p.Met1261Lys
XR_002956289.1:n.4174T>A
NM_001363725.2:c.1631T>A	NP_001350654.1:p.Met544Lys
NM_001371656.1:c.4010T>A	NP_001358585.1:p.Met1337Lys
NM_001374820.1:c.4010T>A	NP_001361749.1:p.Met1337Lys
NM_001374828.1:c.4130T>A MANE Select	NP_001361757.1:p.Met1377Lys
NM_017519.3:c.3971T>A	NP_059989.3:p.Met1324Lys