Canonical Allele Identifier: CA366235289

Gene: ARID1B

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3971T>C	ENSP00000055163.8:p.Met1324Thr
ENST00000414678.8:c.4040T>C	ENSP00000412835.3:p.Met1347Thr
ENST00000637015.2:c.4259T>C	ENSP00000489729.2:p.Met1420Thr
ENST00000346085.10:c.4010T>C	ENSP00000344546.5:p.Met1337Thr
ENST00000350026.10:c.3722T>C	ENSP00000055163.7:p.Met1241Thr
ENST00000414678.7:c.2288T>C	ENSP00000412835.2:p.Met763Thr
ENST00000635849.1:c.1451T>C	ENSP00000490948.1:p.Met484Thr
ENST00000635957.1:c.1082T>C	ENSP00000490385.1:p.Met361Thr
ENST00000636930.2:c.4130T>C MANE Select	ENSP00000490491.2:p.Met1377Thr
ENST00000636940.1:n.2127T>C
ENST00000637015.1:c.1498T>C
ENST00000637568.1:c.1412T>C
ENST00000637741.1:n.796T>C
ENST00000637810.1:c.1472T>C	ENSP00000489636.1:p.Met491Thr
ENST00000637904.1:c.1631T>C	ENSP00000490550.1:p.Met544Thr
ENST00000647938.1:c.3761T>C	ENSP00000498155.1:p.Met1254Thr
ENST00000346085.9:c.3761T>C	ENSP00000344546.4:p.Met1254Thr
ENST00000350026.9:c.3722T>C	ENSP00000055163.7:p.Met1241Thr
ENST00000414678.6:c.2288T>C	ENSP00000412835.2:p.Met763Thr
NM_017519.2:c.3722T>C	NP_059989.2:p.Met1241Thr
NM_020732.3:c.3761T>C	NP_065783.3:p.Met1254Thr
XM_005267069.3:c.3881T>C	XP_005267126.2:p.Met1294Thr
XM_011535984.1:c.2960T>C	XP_011534286.1:p.Met987Thr
XM_011535985.1:c.2780T>C	XP_011534287.1:p.Met927Thr
XM_011535986.1:c.2540T>C	XP_011534288.1:p.Met847Thr
XM_011535987.1:c.2159T>C	XP_011534289.1:p.Met720Thr
XM_011535988.1:c.1022T>C	XP_011534290.1:p.Met341Thr
NM_001346813.1:c.3881T>C	NP_001333742.1:p.Met1294Thr
NM_001363725.1:c.1631T>C	NP_001350654.1:p.Met544Thr
XM_011535984.2:c.4091T>C	XP_011534286.2:p.Met1364Thr
XM_011535988.3:c.1022T>C	XP_011534290.1:p.Met341Thr
XM_017011103.2:c.3992T>C	XP_016866592.1:p.Met1331Thr
XM_017011104.1:c.3962T>C	XP_016866593.1:p.Met1321Thr
XM_017011105.2:c.3932T>C	XP_016866594.1:p.Met1311Thr
XM_017011106.2:c.3803T>C	XP_016866595.1:p.Met1268Thr
XM_017011107.2:c.3782T>C	XP_016866596.1:p.Met1261Thr
XR_002956289.1:n.4174T>C
NM_001363725.2:c.1631T>C	NP_001350654.1:p.Met544Thr
NM_001371656.1:c.4010T>C	NP_001358585.1:p.Met1337Thr
NM_001374820.1:c.4010T>C	NP_001361749.1:p.Met1337Thr
NM_001374828.1:c.4130T>C MANE Select	NP_001361757.1:p.Met1377Thr
NM_017519.3:c.3971T>C	NP_059989.3:p.Met1324Thr