Canonical Allele Identifier: CA4067105

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157133061T>C , CM000668.2:g.157133061T>C	GRCh38
NC_000006.11:g.157454195T>C , CM000668.1:g.157454195T>C	GRCh37
NC_000006.10:g.157495887T>C	NCBI36
NG_032093.1:g.360132T>C
NG_032093.2:g.360132T>C
NG_066624.1:g.362036T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.2615T>C MANE Select	NP_001361757.1:p.Met872Thr
ENST00000636930.2:c.2615T>C MANE Select	ENSP00000490491.2:p.Met872Thr
NM_001346813.1:c.2366T>C	NP_001333742.1:p.Met789Thr
NM_001363725.1:c.116T>C	NP_001350654.1:p.Met39Thr
NM_001363725.2:c.116T>C	NP_001350654.1:p.Met39Thr
NM_001371656.1:c.2654T>C	NP_001358585.1:p.Met885Thr
NM_001374820.1:c.2654T>C	NP_001361749.1:p.Met885Thr
NM_017519.2:c.2366T>C	NP_059989.2:p.Met789Thr
NM_017519.3:c.2615T>C	NP_059989.3:p.Met872Thr
NM_020732.3:c.2405T>C	NP_065783.3:p.Met802Thr
ENST00000319584.10:c.632T>C	ENSP00000313006.6:p.Met211Thr
ENST00000319584.11:c.629T>C	ENSP00000313006.7:p.Met210Thr
ENST00000346085.10:c.2654T>C	ENSP00000344546.5:p.Met885Thr
ENST00000346085.9:c.2405T>C	ENSP00000344546.4:p.Met802Thr
ENST00000350026.10:c.2366T>C	ENSP00000055163.7:p.Met789Thr
ENST00000350026.11:c.2615T>C	ENSP00000055163.8:p.Met872Thr
ENST00000350026.9:c.2366T>C	ENSP00000055163.7:p.Met789Thr
ENST00000414678.6:c.773T>C	ENSP00000412835.2:p.Met258Thr
ENST00000414678.7:c.773T>C	ENSP00000412835.2:p.Met258Thr
ENST00000414678.8:c.2525T>C	ENSP00000412835.3:p.Met842Thr
ENST00000452544.1:n.462T>C
ENST00000452544.2:n.516T>C
ENST00000635849.1:c.83-15563T>C	ENSP00000490948.1:n.83-15563T>C
ENST00000637003.1:c.116T>C	ENSP00000489666.1:p.Met39Thr
ENST00000637015.2:c.2615T>C	ENSP00000489729.2:p.Met872Thr
ENST00000637810.1:c.116T>C	ENSP00000489636.1:p.Met39Thr
ENST00000637904.1:c.116T>C	ENSP00000490550.1:p.Met39Thr
ENST00000647938.1:c.2405T>C	ENSP00000498155.1:p.Met802Thr
ENST00000674190.1:n.1364T>C
XM_005267069.3:c.2366T>C	XP_005267126.2:p.Met789Thr
XM_011535984.1:c.1316T>C	XP_011534286.1:p.Met439Thr
XM_011535984.2:c.2447T>C	XP_011534286.2:p.Met816Thr
XM_011535985.1:c.1283-15563T>C	XP_011534287.1:n.1283-15563T>C
XM_011535986.1:c.896T>C	XP_011534288.1:p.Met299Thr
XM_011535987.1:c.515T>C	XP_011534289.1:p.Met172Thr
XM_017011103.2:c.2447T>C	XP_016866592.1:p.Met816Thr
XM_017011104.1:c.2447T>C	XP_016866593.1:p.Met816Thr
XM_017011105.2:c.2447T>C	XP_016866594.1:p.Met816Thr
XM_017011106.2:c.2447T>C	XP_016866595.1:p.Met816Thr
XM_017011107.2:c.2414-15563T>C	XP_016866596.1:n.2414-15563T>C
XR_002956289.1:n.2530T>C