Canonical Allele Identifier: CA366242452

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522440A>T (hg19) ; chr6:g.157201306A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201306A>T , CM000668.2:g.157201306A>T	GRCh38
NC_000006.11:g.157522440A>T , CM000668.1:g.157522440A>T	GRCh37
NC_000006.10:g.157564132A>T	NCBI36
NG_032093.1:g.428377A>T
NG_032093.2:g.428377A>T
NG_066624.1:g.430281A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4922A>T	ENSP00000055163.8:p.Lys1641Met
ENST00000414678.8:c.4991A>T	ENSP00000412835.3:p.Lys1664Met
ENST00000637015.2:c.5210A>T	ENSP00000489729.2:p.Lys1737Met
ENST00000346085.10:c.4961A>T	ENSP00000344546.5:p.Lys1654Met
ENST00000350026.10:c.4673A>T	ENSP00000055163.7:p.Lys1558Met
ENST00000414678.7:c.3239A>T	ENSP00000412835.2:p.Lys1080Met
ENST00000635849.1:c.2402A>T	ENSP00000490948.1:p.Lys801Met
ENST00000635957.1:c.2033A>T	ENSP00000490385.1:p.Lys678Met
ENST00000636227.1:n.3544A>T
ENST00000636254.1:n.1001A>T
ENST00000636930.2:c.5081A>T MANE Select	ENSP00000490491.2:p.Lys1694Met
ENST00000636940.1:n.3078A>T
ENST00000637015.1:c.2449A>T
ENST00000637568.1:c.2363A>T
ENST00000637741.1:n.1747A>T
ENST00000637810.1:c.2423A>T	ENSP00000489636.1:p.Lys808Met
ENST00000637904.1:c.2582A>T	ENSP00000490550.1:p.Lys861Met
ENST00000647938.1:c.4712A>T	ENSP00000498155.1:p.Lys1571Met
ENST00000346085.9:c.4712A>T	ENSP00000344546.4:p.Lys1571Met
ENST00000350026.9:c.4673A>T	ENSP00000055163.7:p.Lys1558Met
ENST00000414678.6:c.3239A>T	ENSP00000412835.2:p.Lys1080Met
NM_017519.2:c.4673A>T	NP_059989.2:p.Lys1558Met
NM_020732.3:c.4712A>T	NP_065783.3:p.Lys1571Met
XM_005267069.3:c.4832A>T	XP_005267126.2:p.Lys1611Met
XM_011535984.1:c.3911A>T	XP_011534286.1:p.Lys1304Met
XM_011535985.1:c.3731A>T	XP_011534287.1:p.Lys1244Met
XM_011535986.1:c.3491A>T	XP_011534288.1:p.Lys1164Met
XM_011535987.1:c.3110A>T	XP_011534289.1:p.Lys1037Met
XM_011535988.1:c.1973A>T	XP_011534290.1:p.Lys658Met
NM_001346813.1:c.4832A>T	NP_001333742.1:p.Lys1611Met
NM_001363725.1:c.2582A>T	NP_001350654.1:p.Lys861Met
XM_011535984.2:c.5042A>T	XP_011534286.2:p.Lys1681Met
XM_011535988.3:c.1973A>T	XP_011534290.1:p.Lys658Met
XM_017011103.2:c.4943A>T	XP_016866592.1:p.Lys1648Met
XM_017011104.1:c.4913A>T	XP_016866593.1:p.Lys1638Met
XM_017011105.2:c.4883A>T	XP_016866594.1:p.Lys1628Met
XM_017011106.2:c.4754A>T	XP_016866595.1:p.Lys1585Met
XM_017011107.2:c.4733A>T	XP_016866596.1:p.Lys1578Met
XR_002956289.1:n.5028A>T
NM_001363725.2:c.2582A>T	NP_001350654.1:p.Lys861Met
NM_001371656.1:c.4961A>T	NP_001358585.1:p.Lys1654Met
NM_001374820.1:c.4961A>T	NP_001361749.1:p.Lys1654Met
NM_001374828.1:c.5081A>T MANE Select	NP_001361757.1:p.Lys1694Met
NM_017519.3:c.4922A>T	NP_059989.3:p.Lys1641Met