Canonical Allele Identifier: CA366389258

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470060G>A (hg19) ; chr6:g.157148926G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148926G>A , CM000668.2:g.157148926G>A	GRCh38
NC_000006.11:g.157470060G>A , CM000668.1:g.157470060G>A	GRCh37
NC_000006.10:g.157511752G>A	NCBI36
NG_032093.1:g.375997G>A
NG_032093.2:g.375997G>A
NG_066624.1:g.377901G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3064G>A	ENSP00000055163.8:p.Ala1022Thr
ENST00000414678.8:c.2974G>A	ENSP00000412835.3:p.Ala992Thr
ENST00000637015.2:c.3064G>A	ENSP00000489729.2:p.Ala1022Thr
ENST00000319584.11:c.1078G>A	ENSP00000313006.7:p.Ala360Thr
ENST00000346085.10:c.3103G>A	ENSP00000344546.5:p.Ala1035Thr
ENST00000350026.10:c.2815G>A	ENSP00000055163.7:p.Ala939Thr
ENST00000414678.7:c.1222G>A	ENSP00000412835.2:p.Ala408Thr
ENST00000452544.2:n.965G>A
ENST00000635849.1:c.385G>A	ENSP00000490948.1:p.Ala129Thr
ENST00000635957.1:c.19G>A	ENSP00000490385.1:p.Ala7Thr
ENST00000636426.1:n.198G>A
ENST00000636930.2:c.3064G>A MANE Select	ENSP00000490491.2:p.Ala1022Thr
ENST00000637015.1:c.303G>A
ENST00000637568.1:c.107G>A
ENST00000637810.1:c.565G>A	ENSP00000489636.1:p.Ala189Thr
ENST00000637904.1:c.565G>A	ENSP00000490550.1:p.Ala189Thr
ENST00000647938.1:c.2854G>A	ENSP00000498155.1:p.Ala952Thr
ENST00000674190.1:n.1813G>A
ENST00000319584.10:c.1081G>A	ENSP00000313006.6:p.Ala361Thr
ENST00000346085.9:c.2854G>A	ENSP00000344546.4:p.Ala952Thr
ENST00000350026.9:c.2815G>A	ENSP00000055163.7:p.Ala939Thr
ENST00000400790.3:c.16G>A	ENSP00000383596.3:p.Ala6Thr
ENST00000414678.6:c.1222G>A	ENSP00000412835.2:p.Ala408Thr
ENST00000452544.1:n.911G>A
ENST00000478761.3:c.137G>A
NM_017519.2:c.2815G>A	NP_059989.2:p.Ala939Thr
NM_020732.3:c.2854G>A	NP_065783.3:p.Ala952Thr
XM_005267069.3:c.2815G>A	XP_005267126.2:p.Ala939Thr
XM_011535984.1:c.1765G>A	XP_011534286.1:p.Ala589Thr
XM_011535985.1:c.1585G>A	XP_011534287.1:p.Ala529Thr
XM_011535986.1:c.1345G>A	XP_011534288.1:p.Ala449Thr
XM_011535987.1:c.964G>A	XP_011534289.1:p.Ala322Thr
XM_011535988.1:c.-20+15719G>A	XP_011534290.1:n.-20+15719G>A
NM_001346813.1:c.2815G>A	NP_001333742.1:p.Ala939Thr
NM_001363725.1:c.565G>A	NP_001350654.1:p.Ala189Thr
XM_011535984.2:c.2896G>A	XP_011534286.2:p.Ala966Thr
XM_011535988.3:c.-20+15719G>A	XP_011534290.1:n.-20+15719G>A
XM_017011103.2:c.2896G>A	XP_016866592.1:p.Ala966Thr
XM_017011104.1:c.2896G>A	XP_016866593.1:p.Ala966Thr
XM_017011105.2:c.2896G>A	XP_016866594.1:p.Ala966Thr
XM_017011106.2:c.2896G>A	XP_016866595.1:p.Ala966Thr
XM_017011107.2:c.2716G>A	XP_016866596.1:p.Ala906Thr
XR_002956289.1:n.2979G>A
NM_001363725.2:c.565G>A	NP_001350654.1:p.Ala189Thr
NM_001371656.1:c.3103G>A	NP_001358585.1:p.Ala1035Thr
NM_001374820.1:c.3103G>A	NP_001361749.1:p.Ala1035Thr
NM_001374828.1:c.3064G>A MANE Select	NP_001361757.1:p.Ala1022Thr
NM_017519.3:c.3064G>A	NP_059989.3:p.Ala1022Thr