Canonical Allele Identifier: CA366241952

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522227T>A (hg19) ; chr6:g.157201093T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201093T>A , CM000668.2:g.157201093T>A	GRCh38
NC_000006.11:g.157522227T>A , CM000668.1:g.157522227T>A	GRCh37
NC_000006.10:g.157563919T>A	NCBI36
NG_032093.1:g.428164T>A
NG_032093.2:g.428164T>A
NG_066624.1:g.430068T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4709T>A	ENSP00000055163.8:p.Met1570Lys
ENST00000414678.8:c.4778T>A	ENSP00000412835.3:p.Met1593Lys
ENST00000637015.2:c.4997T>A	ENSP00000489729.2:p.Met1666Lys
ENST00000346085.10:c.4748T>A	ENSP00000344546.5:p.Met1583Lys
ENST00000350026.10:c.4460T>A	ENSP00000055163.7:p.Met1487Lys
ENST00000414678.7:c.3026T>A	ENSP00000412835.2:p.Met1009Lys
ENST00000635849.1:c.2189T>A	ENSP00000490948.1:p.Met730Lys
ENST00000635957.1:c.1820T>A	ENSP00000490385.1:p.Met607Lys
ENST00000636227.1:n.3331T>A
ENST00000636254.1:n.788T>A
ENST00000636930.2:c.4868T>A MANE Select	ENSP00000490491.2:p.Met1623Lys
ENST00000636940.1:n.2865T>A
ENST00000637015.1:c.2236T>A
ENST00000637568.1:c.2150T>A
ENST00000637741.1:n.1534T>A
ENST00000637810.1:c.2210T>A	ENSP00000489636.1:p.Met737Lys
ENST00000637904.1:c.2369T>A	ENSP00000490550.1:p.Met790Lys
ENST00000647938.1:c.4499T>A	ENSP00000498155.1:p.Met1500Lys
ENST00000346085.9:c.4499T>A	ENSP00000344546.4:p.Met1500Lys
ENST00000350026.9:c.4460T>A	ENSP00000055163.7:p.Met1487Lys
ENST00000414678.6:c.3026T>A	ENSP00000412835.2:p.Met1009Lys
NM_017519.2:c.4460T>A	NP_059989.2:p.Met1487Lys
NM_020732.3:c.4499T>A	NP_065783.3:p.Met1500Lys
XM_005267069.3:c.4619T>A	XP_005267126.2:p.Met1540Lys
XM_011535984.1:c.3698T>A	XP_011534286.1:p.Met1233Lys
XM_011535985.1:c.3518T>A	XP_011534287.1:p.Met1173Lys
XM_011535986.1:c.3278T>A	XP_011534288.1:p.Met1093Lys
XM_011535987.1:c.2897T>A	XP_011534289.1:p.Met966Lys
XM_011535988.1:c.1760T>A	XP_011534290.1:p.Met587Lys
NM_001346813.1:c.4619T>A	NP_001333742.1:p.Met1540Lys
NM_001363725.1:c.2369T>A	NP_001350654.1:p.Met790Lys
XM_011535984.2:c.4829T>A	XP_011534286.2:p.Met1610Lys
XM_011535988.3:c.1760T>A	XP_011534290.1:p.Met587Lys
XM_017011103.2:c.4730T>A	XP_016866592.1:p.Met1577Lys
XM_017011104.1:c.4700T>A	XP_016866593.1:p.Met1567Lys
XM_017011105.2:c.4670T>A	XP_016866594.1:p.Met1557Lys
XM_017011106.2:c.4541T>A	XP_016866595.1:p.Met1514Lys
XM_017011107.2:c.4520T>A	XP_016866596.1:p.Met1507Lys
XR_002956289.1:n.4815T>A
NM_001363725.2:c.2369T>A	NP_001350654.1:p.Met790Lys
NM_001371656.1:c.4748T>A	NP_001358585.1:p.Met1583Lys
NM_001374820.1:c.4748T>A	NP_001361749.1:p.Met1583Lys
NM_001374828.1:c.4868T>A MANE Select	NP_001361757.1:p.Met1623Lys
NM_017519.3:c.4709T>A	NP_059989.3:p.Met1570Lys