Canonical Allele Identifier: CA366242439

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128375776
• MyVariant Identifiers: chr6:g.157522434C>T (hg19) ; chr6:g.157201300C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201300C>T , CM000668.2:g.157201300C>T	GRCh38
NC_000006.11:g.157522434C>T , CM000668.1:g.157522434C>T	GRCh37
NC_000006.10:g.157564126C>T	NCBI36
NG_032093.1:g.428371C>T
NG_032093.2:g.428371C>T
NG_066624.1:g.430275C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4916C>T	ENSP00000055163.8:p.Pro1639Leu
ENST00000414678.8:c.4985C>T	ENSP00000412835.3:p.Pro1662Leu
ENST00000637015.2:c.5204C>T	ENSP00000489729.2:p.Pro1735Leu
ENST00000346085.10:c.4955C>T	ENSP00000344546.5:p.Pro1652Leu
ENST00000350026.10:c.4667C>T	ENSP00000055163.7:p.Pro1556Leu
ENST00000414678.7:c.3233C>T	ENSP00000412835.2:p.Pro1078Leu
ENST00000635849.1:c.2396C>T	ENSP00000490948.1:p.Pro799Leu
ENST00000635957.1:c.2027C>T	ENSP00000490385.1:p.Pro676Leu
ENST00000636227.1:n.3538C>T
ENST00000636254.1:n.995C>T
ENST00000636930.2:c.5075C>T MANE Select	ENSP00000490491.2:p.Pro1692Leu
ENST00000636940.1:n.3072C>T
ENST00000637015.1:c.2443C>T
ENST00000637568.1:c.2357C>T
ENST00000637741.1:n.1741C>T
ENST00000637810.1:c.2417C>T	ENSP00000489636.1:p.Pro806Leu
ENST00000637904.1:c.2576C>T	ENSP00000490550.1:p.Pro859Leu
ENST00000647938.1:c.4706C>T	ENSP00000498155.1:p.Pro1569Leu
ENST00000346085.9:c.4706C>T	ENSP00000344546.4:p.Pro1569Leu
ENST00000350026.9:c.4667C>T	ENSP00000055163.7:p.Pro1556Leu
ENST00000414678.6:c.3233C>T	ENSP00000412835.2:p.Pro1078Leu
NM_017519.2:c.4667C>T	NP_059989.2:p.Pro1556Leu
NM_020732.3:c.4706C>T	NP_065783.3:p.Pro1569Leu
XM_005267069.3:c.4826C>T	XP_005267126.2:p.Pro1609Leu
XM_011535984.1:c.3905C>T	XP_011534286.1:p.Pro1302Leu
XM_011535985.1:c.3725C>T	XP_011534287.1:p.Pro1242Leu
XM_011535986.1:c.3485C>T	XP_011534288.1:p.Pro1162Leu
XM_011535987.1:c.3104C>T	XP_011534289.1:p.Pro1035Leu
XM_011535988.1:c.1967C>T	XP_011534290.1:p.Pro656Leu
NM_001346813.1:c.4826C>T	NP_001333742.1:p.Pro1609Leu
NM_001363725.1:c.2576C>T	NP_001350654.1:p.Pro859Leu
XM_011535984.2:c.5036C>T	XP_011534286.2:p.Pro1679Leu
XM_011535988.3:c.1967C>T	XP_011534290.1:p.Pro656Leu
XM_017011103.2:c.4937C>T	XP_016866592.1:p.Pro1646Leu
XM_017011104.1:c.4907C>T	XP_016866593.1:p.Pro1636Leu
XM_017011105.2:c.4877C>T	XP_016866594.1:p.Pro1626Leu
XM_017011106.2:c.4748C>T	XP_016866595.1:p.Pro1583Leu
XM_017011107.2:c.4727C>T	XP_016866596.1:p.Pro1576Leu
XR_002956289.1:n.5022C>T
NM_001363725.2:c.2576C>T	NP_001350654.1:p.Pro859Leu
NM_001371656.1:c.4955C>T	NP_001358585.1:p.Pro1652Leu
NM_001374820.1:c.4955C>T	NP_001361749.1:p.Pro1652Leu
NM_001374828.1:c.5075C>T MANE Select	NP_001361757.1:p.Pro1692Leu
NM_017519.3:c.4916C>T	NP_059989.3:p.Pro1639Leu