Canonical Allele Identifier: CA366242582

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522466A>G (hg19) ; chr6:g.157201332A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201332A>G , CM000668.2:g.157201332A>G	GRCh38
NC_000006.11:g.157522466A>G , CM000668.1:g.157522466A>G	GRCh37
NC_000006.10:g.157564158A>G	NCBI36
NG_032093.1:g.428403A>G
NG_032093.2:g.428403A>G
NG_066624.1:g.430307A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4948A>G	ENSP00000055163.8:p.Met1650Val
ENST00000414678.8:c.5017A>G	ENSP00000412835.3:p.Met1673Val
ENST00000637015.2:c.5236A>G	ENSP00000489729.2:p.Met1746Val
ENST00000346085.10:c.4987A>G	ENSP00000344546.5:p.Met1663Val
ENST00000350026.10:c.4699A>G	ENSP00000055163.7:p.Met1567Val
ENST00000414678.7:c.3265A>G	ENSP00000412835.2:p.Met1089Val
ENST00000635849.1:c.2428A>G	ENSP00000490948.1:p.Met810Val
ENST00000635957.1:c.2059A>G	ENSP00000490385.1:p.Met687Val
ENST00000636227.1:n.3570A>G
ENST00000636254.1:n.1027A>G
ENST00000636930.2:c.5107A>G MANE Select	ENSP00000490491.2:p.Met1703Val
ENST00000636940.1:n.3104A>G
ENST00000637015.1:c.2475A>G
ENST00000637568.1:c.2389A>G
ENST00000637741.1:n.1773A>G
ENST00000637810.1:c.2449A>G	ENSP00000489636.1:p.Met817Val
ENST00000637904.1:c.2608A>G	ENSP00000490550.1:p.Met870Val
ENST00000647938.1:c.4738A>G	ENSP00000498155.1:p.Met1580Val
ENST00000346085.9:c.4738A>G	ENSP00000344546.4:p.Met1580Val
ENST00000350026.9:c.4699A>G	ENSP00000055163.7:p.Met1567Val
ENST00000414678.6:c.3265A>G	ENSP00000412835.2:p.Met1089Val
NM_017519.2:c.4699A>G	NP_059989.2:p.Met1567Val
NM_020732.3:c.4738A>G	NP_065783.3:p.Met1580Val
XM_005267069.3:c.4858A>G	XP_005267126.2:p.Met1620Val
XM_011535984.1:c.3937A>G	XP_011534286.1:p.Met1313Val
XM_011535985.1:c.3757A>G	XP_011534287.1:p.Met1253Val
XM_011535986.1:c.3517A>G	XP_011534288.1:p.Met1173Val
XM_011535987.1:c.3136A>G	XP_011534289.1:p.Met1046Val
XM_011535988.1:c.1999A>G	XP_011534290.1:p.Met667Val
NM_001346813.1:c.4858A>G	NP_001333742.1:p.Met1620Val
NM_001363725.1:c.2608A>G	NP_001350654.1:p.Met870Val
XM_011535984.2:c.5068A>G	XP_011534286.2:p.Met1690Val
XM_011535988.3:c.1999A>G	XP_011534290.1:p.Met667Val
XM_017011103.2:c.4969A>G	XP_016866592.1:p.Met1657Val
XM_017011104.1:c.4939A>G	XP_016866593.1:p.Met1647Val
XM_017011105.2:c.4909A>G	XP_016866594.1:p.Met1637Val
XM_017011106.2:c.4780A>G	XP_016866595.1:p.Met1594Val
XM_017011107.2:c.4759A>G	XP_016866596.1:p.Met1587Val
XR_002956289.1:n.5054A>G
NM_001363725.2:c.2608A>G	NP_001350654.1:p.Met870Val
NM_001371656.1:c.4987A>G	NP_001358585.1:p.Met1663Val
NM_001374820.1:c.4987A>G	NP_001361749.1:p.Met1663Val
NM_001374828.1:c.5107A>G MANE Select	NP_001361757.1:p.Met1703Val
NM_017519.3:c.4948A>G	NP_059989.3:p.Met1650Val