Canonical Allele Identifier: CA366242038

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522252T>G (hg19) ; chr6:g.157201118T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201118T>G , CM000668.2:g.157201118T>G	GRCh38
NC_000006.11:g.157522252T>G , CM000668.1:g.157522252T>G	GRCh37
NC_000006.10:g.157563944T>G	NCBI36
NG_032093.1:g.428189T>G
NG_032093.2:g.428189T>G
NG_066624.1:g.430093T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4734T>G	ENSP00000055163.8:p.His1578Gln
ENST00000414678.8:c.4803T>G	ENSP00000412835.3:p.His1601Gln
ENST00000637015.2:c.5022T>G	ENSP00000489729.2:p.His1674Gln
ENST00000346085.10:c.4773T>G	ENSP00000344546.5:p.His1591Gln
ENST00000350026.10:c.4485T>G	ENSP00000055163.7:p.His1495Gln
ENST00000414678.7:c.3051T>G	ENSP00000412835.2:p.His1017Gln
ENST00000635849.1:c.2214T>G	ENSP00000490948.1:p.His738Gln
ENST00000635957.1:c.1845T>G	ENSP00000490385.1:p.His615Gln
ENST00000636227.1:n.3356T>G
ENST00000636254.1:n.813T>G
ENST00000636930.2:c.4893T>G MANE Select	ENSP00000490491.2:p.His1631Gln
ENST00000636940.1:n.2890T>G
ENST00000637015.1:c.2261T>G
ENST00000637568.1:c.2175T>G
ENST00000637741.1:n.1559T>G
ENST00000637810.1:c.2235T>G	ENSP00000489636.1:p.His745Gln
ENST00000637904.1:c.2394T>G	ENSP00000490550.1:p.His798Gln
ENST00000647938.1:c.4524T>G	ENSP00000498155.1:p.His1508Gln
ENST00000346085.9:c.4524T>G	ENSP00000344546.4:p.His1508Gln
ENST00000350026.9:c.4485T>G	ENSP00000055163.7:p.His1495Gln
ENST00000414678.6:c.3051T>G	ENSP00000412835.2:p.His1017Gln
NM_017519.2:c.4485T>G	NP_059989.2:p.His1495Gln
NM_020732.3:c.4524T>G	NP_065783.3:p.His1508Gln
XM_005267069.3:c.4644T>G	XP_005267126.2:p.His1548Gln
XM_011535984.1:c.3723T>G	XP_011534286.1:p.His1241Gln
XM_011535985.1:c.3543T>G	XP_011534287.1:p.His1181Gln
XM_011535986.1:c.3303T>G	XP_011534288.1:p.His1101Gln
XM_011535987.1:c.2922T>G	XP_011534289.1:p.His974Gln
XM_011535988.1:c.1785T>G	XP_011534290.1:p.His595Gln
NM_001346813.1:c.4644T>G	NP_001333742.1:p.His1548Gln
NM_001363725.1:c.2394T>G	NP_001350654.1:p.His798Gln
XM_011535984.2:c.4854T>G	XP_011534286.2:p.His1618Gln
XM_011535988.3:c.1785T>G	XP_011534290.1:p.His595Gln
XM_017011103.2:c.4755T>G	XP_016866592.1:p.His1585Gln
XM_017011104.1:c.4725T>G	XP_016866593.1:p.His1575Gln
XM_017011105.2:c.4695T>G	XP_016866594.1:p.His1565Gln
XM_017011106.2:c.4566T>G	XP_016866595.1:p.His1522Gln
XM_017011107.2:c.4545T>G	XP_016866596.1:p.His1515Gln
XR_002956289.1:n.4840T>G
NM_001363725.2:c.2394T>G	NP_001350654.1:p.His798Gln
NM_001371656.1:c.4773T>G	NP_001358585.1:p.His1591Gln
NM_001374820.1:c.4773T>G	NP_001361749.1:p.His1591Gln
NM_001374828.1:c.4893T>G MANE Select	NP_001361757.1:p.His1631Gln
NM_017519.3:c.4734T>G	NP_059989.3:p.His1578Gln