Canonical Allele Identifier: CA366241931

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201090-T-A
• MyVariant Identifiers: chr6:g.157522224T>A (hg19) ; chr6:g.157201090T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201090T>A , CM000668.2:g.157201090T>A	GRCh38
NC_000006.11:g.157522224T>A , CM000668.1:g.157522224T>A	GRCh37
NC_000006.10:g.157563916T>A	NCBI36
NG_032093.1:g.428161T>A
NG_032093.2:g.428161T>A
NG_066624.1:g.430065T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4706T>A	ENSP00000055163.8:p.Met1569Lys
ENST00000414678.8:c.4775T>A	ENSP00000412835.3:p.Met1592Lys
ENST00000637015.2:c.4994T>A	ENSP00000489729.2:p.Met1665Lys
ENST00000346085.10:c.4745T>A	ENSP00000344546.5:p.Met1582Lys
ENST00000350026.10:c.4457T>A	ENSP00000055163.7:p.Met1486Lys
ENST00000414678.7:c.3023T>A	ENSP00000412835.2:p.Met1008Lys
ENST00000635849.1:c.2186T>A	ENSP00000490948.1:p.Met729Lys
ENST00000635957.1:c.1817T>A	ENSP00000490385.1:p.Met606Lys
ENST00000636227.1:n.3328T>A
ENST00000636254.1:n.785T>A
ENST00000636930.2:c.4865T>A MANE Select	ENSP00000490491.2:p.Met1622Lys
ENST00000636940.1:n.2862T>A
ENST00000637015.1:c.2233T>A
ENST00000637568.1:c.2147T>A
ENST00000637741.1:n.1531T>A
ENST00000637810.1:c.2207T>A	ENSP00000489636.1:p.Met736Lys
ENST00000637904.1:c.2366T>A	ENSP00000490550.1:p.Met789Lys
ENST00000647938.1:c.4496T>A	ENSP00000498155.1:p.Met1499Lys
ENST00000346085.9:c.4496T>A	ENSP00000344546.4:p.Met1499Lys
ENST00000350026.9:c.4457T>A	ENSP00000055163.7:p.Met1486Lys
ENST00000414678.6:c.3023T>A	ENSP00000412835.2:p.Met1008Lys
NM_017519.2:c.4457T>A	NP_059989.2:p.Met1486Lys
NM_020732.3:c.4496T>A	NP_065783.3:p.Met1499Lys
XM_005267069.3:c.4616T>A	XP_005267126.2:p.Met1539Lys
XM_011535984.1:c.3695T>A	XP_011534286.1:p.Met1232Lys
XM_011535985.1:c.3515T>A	XP_011534287.1:p.Met1172Lys
XM_011535986.1:c.3275T>A	XP_011534288.1:p.Met1092Lys
XM_011535987.1:c.2894T>A	XP_011534289.1:p.Met965Lys
XM_011535988.1:c.1757T>A	XP_011534290.1:p.Met586Lys
NM_001346813.1:c.4616T>A	NP_001333742.1:p.Met1539Lys
NM_001363725.1:c.2366T>A	NP_001350654.1:p.Met789Lys
XM_011535984.2:c.4826T>A	XP_011534286.2:p.Met1609Lys
XM_011535988.3:c.1757T>A	XP_011534290.1:p.Met586Lys
XM_017011103.2:c.4727T>A	XP_016866592.1:p.Met1576Lys
XM_017011104.1:c.4697T>A	XP_016866593.1:p.Met1566Lys
XM_017011105.2:c.4667T>A	XP_016866594.1:p.Met1556Lys
XM_017011106.2:c.4538T>A	XP_016866595.1:p.Met1513Lys
XM_017011107.2:c.4517T>A	XP_016866596.1:p.Met1506Lys
XR_002956289.1:n.4812T>A
NM_001363725.2:c.2366T>A	NP_001350654.1:p.Met789Lys
NM_001371656.1:c.4745T>A	NP_001358585.1:p.Met1582Lys
NM_001374820.1:c.4745T>A	NP_001361749.1:p.Met1582Lys
NM_001374828.1:c.4865T>A MANE Select	NP_001361757.1:p.Met1622Lys
NM_017519.3:c.4706T>A	NP_059989.3:p.Met1569Lys