Canonical Allele Identifier: CA366247891

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207035T>C , CM000668.2:g.157207035T>C	GRCh38
NC_000006.11:g.157528169T>C , CM000668.1:g.157528169T>C	GRCh37
NC_000006.10:g.157569861T>C	NCBI36
NG_032093.1:g.434106T>C
NG_032093.2:g.434106T>C
NG_066624.1:g.436010T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.6263T>C MANE Select	NP_001361757.1:p.Met2088Thr
ENST00000636930.2:c.6263T>C MANE Select	ENSP00000490491.2:p.Met2088Thr
NM_001346813.1:c.6014T>C	NP_001333742.1:p.Met2005Thr
NM_001363725.1:c.3764T>C	NP_001350654.1:p.Met1255Thr
NM_001363725.2:c.3764T>C	NP_001350654.1:p.Met1255Thr
NM_001371656.1:c.6143T>C	NP_001358585.1:p.Met2048Thr
NM_001374820.1:c.6143T>C	NP_001361749.1:p.Met2048Thr
NM_017519.2:c.5855T>C	NP_059989.2:p.Met1952Thr
NM_017519.3:c.6104T>C	NP_059989.3:p.Met2035Thr
NM_020732.3:c.5894T>C	NP_065783.3:p.Met1965Thr
ENST00000346085.10:c.6143T>C	ENSP00000344546.5:p.Met2048Thr
ENST00000346085.9:c.5894T>C	ENSP00000344546.4:p.Met1965Thr
ENST00000350026.10:c.5855T>C	ENSP00000055163.7:p.Met1952Thr
ENST00000350026.11:c.6104T>C	ENSP00000055163.8:p.Met2035Thr
ENST00000350026.9:c.5855T>C	ENSP00000055163.7:p.Met1952Thr
ENST00000414678.6:c.4421T>C	ENSP00000412835.2:p.Met1474Thr
ENST00000414678.7:c.4421T>C	ENSP00000412835.2:p.Met1474Thr
ENST00000414678.8:c.6173T>C	ENSP00000412835.3:p.Met2058Thr
ENST00000635849.1:c.3584T>C	ENSP00000490948.1:p.Met1195Thr
ENST00000635928.1:c.419T>C	ENSP00000489717.1:p.Met140Thr
ENST00000635957.1:c.3215T>C	ENSP00000490385.1:p.Met1072Thr
ENST00000636227.1:n.4726T>C
ENST00000636254.1:n.2183T>C
ENST00000636940.1:n.4260T>C
ENST00000637015.1:c.3631T>C
ENST00000637015.2:c.6392T>C	ENSP00000489729.2:p.Met2131Thr
ENST00000637568.1:c.3545T>C
ENST00000637741.1:n.2929T>C
ENST00000637810.1:c.3605T>C	ENSP00000489636.1:p.Met1202Thr
ENST00000637904.1:c.3764T>C	ENSP00000490550.1:p.Met1255Thr
ENST00000637933.1:n.3378T>C
ENST00000647938.1:c.5894T>C	ENSP00000498155.1:p.Met1965Thr
XM_005267069.3:c.6014T>C	XP_005267126.2:p.Met2005Thr
XM_011535984.1:c.5093T>C	XP_011534286.1:p.Met1698Thr
XM_011535984.2:c.6224T>C	XP_011534286.2:p.Met2075Thr
XM_011535985.1:c.4913T>C	XP_011534287.1:p.Met1638Thr
XM_011535986.1:c.4673T>C	XP_011534288.1:p.Met1558Thr
XM_011535987.1:c.4292T>C	XP_011534289.1:p.Met1431Thr
XM_011535988.1:c.3155T>C	XP_011534290.1:p.Met1052Thr
XM_011535988.3:c.3155T>C	XP_011534290.1:p.Met1052Thr
XM_017011103.2:c.6125T>C	XP_016866592.1:p.Met2042Thr
XM_017011104.1:c.6095T>C	XP_016866593.1:p.Met2032Thr
XM_017011105.2:c.6065T>C	XP_016866594.1:p.Met2022Thr
XM_017011106.2:c.5936T>C	XP_016866595.1:p.Met1979Thr
XM_017011107.2:c.5915T>C	XP_016866596.1:p.Met1972Thr
XR_002956289.1:n.6210T>C