Canonical Allele Identifier: CA366241937

Gene: ARID1B

Linked Data

• dbSNP Id: rs1391970327
• gnomAD v4: 6-157201091-G-A
• MyVariant Identifiers: chr6:g.157522225G>A (hg19) ; chr6:g.157201091G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201091G>A , CM000668.2:g.157201091G>A	GRCh38
NC_000006.11:g.157522225G>A , CM000668.1:g.157522225G>A	GRCh37
NC_000006.10:g.157563917G>A	NCBI36
NG_032093.1:g.428162G>A
NG_032093.2:g.428162G>A
NG_066624.1:g.430066G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4707G>A	ENSP00000055163.8:p.Met1569Ile
ENST00000414678.8:c.4776G>A	ENSP00000412835.3:p.Met1592Ile
ENST00000637015.2:c.4995G>A	ENSP00000489729.2:p.Met1665Ile
ENST00000346085.10:c.4746G>A	ENSP00000344546.5:p.Met1582Ile
ENST00000350026.10:c.4458G>A	ENSP00000055163.7:p.Met1486Ile
ENST00000414678.7:c.3024G>A	ENSP00000412835.2:p.Met1008Ile
ENST00000635849.1:c.2187G>A	ENSP00000490948.1:p.Met729Ile
ENST00000635957.1:c.1818G>A	ENSP00000490385.1:p.Met606Ile
ENST00000636227.1:n.3329G>A
ENST00000636254.1:n.786G>A
ENST00000636930.2:c.4866G>A MANE Select	ENSP00000490491.2:p.Met1622Ile
ENST00000636940.1:n.2863G>A
ENST00000637015.1:c.2234G>A
ENST00000637568.1:c.2148G>A
ENST00000637741.1:n.1532G>A
ENST00000637810.1:c.2208G>A	ENSP00000489636.1:p.Met736Ile
ENST00000637904.1:c.2367G>A	ENSP00000490550.1:p.Met789Ile
ENST00000647938.1:c.4497G>A	ENSP00000498155.1:p.Met1499Ile
ENST00000346085.9:c.4497G>A	ENSP00000344546.4:p.Met1499Ile
ENST00000350026.9:c.4458G>A	ENSP00000055163.7:p.Met1486Ile
ENST00000414678.6:c.3024G>A	ENSP00000412835.2:p.Met1008Ile
NM_017519.2:c.4458G>A	NP_059989.2:p.Met1486Ile
NM_020732.3:c.4497G>A	NP_065783.3:p.Met1499Ile
XM_005267069.3:c.4617G>A	XP_005267126.2:p.Met1539Ile
XM_011535984.1:c.3696G>A	XP_011534286.1:p.Met1232Ile
XM_011535985.1:c.3516G>A	XP_011534287.1:p.Met1172Ile
XM_011535986.1:c.3276G>A	XP_011534288.1:p.Met1092Ile
XM_011535987.1:c.2895G>A	XP_011534289.1:p.Met965Ile
XM_011535988.1:c.1758G>A	XP_011534290.1:p.Met586Ile
NM_001346813.1:c.4617G>A	NP_001333742.1:p.Met1539Ile
NM_001363725.1:c.2367G>A	NP_001350654.1:p.Met789Ile
XM_011535984.2:c.4827G>A	XP_011534286.2:p.Met1609Ile
XM_011535988.3:c.1758G>A	XP_011534290.1:p.Met586Ile
XM_017011103.2:c.4728G>A	XP_016866592.1:p.Met1576Ile
XM_017011104.1:c.4698G>A	XP_016866593.1:p.Met1566Ile
XM_017011105.2:c.4668G>A	XP_016866594.1:p.Met1556Ile
XM_017011106.2:c.4539G>A	XP_016866595.1:p.Met1513Ile
XM_017011107.2:c.4518G>A	XP_016866596.1:p.Met1506Ile
XR_002956289.1:n.4813G>A
NM_001363725.2:c.2367G>A	NP_001350654.1:p.Met789Ile
NM_001371656.1:c.4746G>A	NP_001358585.1:p.Met1582Ile
NM_001374820.1:c.4746G>A	NP_001361749.1:p.Met1582Ile
NM_001374828.1:c.4866G>A MANE Select	NP_001361757.1:p.Met1622Ile
NM_017519.3:c.4707G>A	NP_059989.3:p.Met1569Ile