Canonical Allele Identifier: CA366240902

Gene: ARID1B

Linked Data

• dbSNP Id: rs1583500373
• gnomAD v4: 6-157200775-T-G
• MyVariant Identifiers: chr6:g.157521909T>G (hg19) ; chr6:g.157200775T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200775T>G , CM000668.2:g.157200775T>G	GRCh38
NC_000006.11:g.157521909T>G , CM000668.1:g.157521909T>G	GRCh37
NC_000006.10:g.157563601T>G	NCBI36
NG_032093.1:g.427846T>G
NG_032093.2:g.427846T>G
NG_066624.1:g.429750T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4391T>G	ENSP00000055163.8:p.Met1464Arg
ENST00000414678.8:c.4460T>G	ENSP00000412835.3:p.Met1487Arg
ENST00000637015.2:c.4679T>G	ENSP00000489729.2:p.Met1560Arg
ENST00000346085.10:c.4430T>G	ENSP00000344546.5:p.Met1477Arg
ENST00000350026.10:c.4142T>G	ENSP00000055163.7:p.Met1381Arg
ENST00000414678.7:c.2708T>G	ENSP00000412835.2:p.Met903Arg
ENST00000635849.1:c.1871T>G	ENSP00000490948.1:p.Met624Arg
ENST00000635957.1:c.1502T>G	ENSP00000490385.1:p.Met501Arg
ENST00000636227.1:n.3013T>G
ENST00000636254.1:n.470T>G
ENST00000636930.2:c.4550T>G MANE Select	ENSP00000490491.2:p.Met1517Arg
ENST00000636940.1:n.2547T>G
ENST00000637015.1:c.1918T>G
ENST00000637568.1:c.1832T>G
ENST00000637741.1:n.1216T>G
ENST00000637810.1:c.1892T>G	ENSP00000489636.1:p.Met631Arg
ENST00000637904.1:c.2051T>G	ENSP00000490550.1:p.Met684Arg
ENST00000647938.1:c.4181T>G	ENSP00000498155.1:p.Met1394Arg
ENST00000346085.9:c.4181T>G	ENSP00000344546.4:p.Met1394Arg
ENST00000350026.9:c.4142T>G	ENSP00000055163.7:p.Met1381Arg
ENST00000414678.6:c.2708T>G	ENSP00000412835.2:p.Met903Arg
NM_017519.2:c.4142T>G	NP_059989.2:p.Met1381Arg
NM_020732.3:c.4181T>G	NP_065783.3:p.Met1394Arg
XM_005267069.3:c.4301T>G	XP_005267126.2:p.Met1434Arg
XM_011535984.1:c.3380T>G	XP_011534286.1:p.Met1127Arg
XM_011535985.1:c.3200T>G	XP_011534287.1:p.Met1067Arg
XM_011535986.1:c.2960T>G	XP_011534288.1:p.Met987Arg
XM_011535987.1:c.2579T>G	XP_011534289.1:p.Met860Arg
XM_011535988.1:c.1442T>G	XP_011534290.1:p.Met481Arg
NM_001346813.1:c.4301T>G	NP_001333742.1:p.Met1434Arg
NM_001363725.1:c.2051T>G	NP_001350654.1:p.Met684Arg
XM_011535984.2:c.4511T>G	XP_011534286.2:p.Met1504Arg
XM_011535988.3:c.1442T>G	XP_011534290.1:p.Met481Arg
XM_017011103.2:c.4412T>G	XP_016866592.1:p.Met1471Arg
XM_017011104.1:c.4382T>G	XP_016866593.1:p.Met1461Arg
XM_017011105.2:c.4352T>G	XP_016866594.1:p.Met1451Arg
XM_017011106.2:c.4223T>G	XP_016866595.1:p.Met1408Arg
XM_017011107.2:c.4202T>G	XP_016866596.1:p.Met1401Arg
XR_002956289.1:n.4497T>G
NM_001363725.2:c.2051T>G	NP_001350654.1:p.Met684Arg
NM_001371656.1:c.4430T>G	NP_001358585.1:p.Met1477Arg
NM_001374820.1:c.4430T>G	NP_001361749.1:p.Met1477Arg
NM_001374828.1:c.4550T>G MANE Select	NP_001361757.1:p.Met1517Arg
NM_017519.3:c.4391T>G	NP_059989.3:p.Met1464Arg