Canonical Allele Identifier: CA366242624

Gene: ARID1B

Linked Data

• dbSNP Id: rs1554235953
• MyVariant Identifiers: chr6:g.157522472A>T (hg19) ; chr6:g.157201338A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201338A>T , CM000668.2:g.157201338A>T	GRCh38
NC_000006.11:g.157522472A>T , CM000668.1:g.157522472A>T	GRCh37
NC_000006.10:g.157564164A>T	NCBI36
NG_032093.1:g.428409A>T
NG_032093.2:g.428409A>T
NG_066624.1:g.430313A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4954A>T	ENSP00000055163.8:p.Lys1652Ter
ENST00000414678.8:c.5023A>T	ENSP00000412835.3:p.Lys1675Ter
ENST00000637015.2:c.5242A>T	ENSP00000489729.2:p.Lys1748Ter
ENST00000346085.10:c.4993A>T	ENSP00000344546.5:p.Lys1665Ter
ENST00000350026.10:c.4705A>T	ENSP00000055163.7:p.Lys1569Ter
ENST00000414678.7:c.3271A>T	ENSP00000412835.2:p.Lys1091Ter
ENST00000635849.1:c.2434A>T	ENSP00000490948.1:p.Lys812Ter
ENST00000635957.1:c.2065A>T	ENSP00000490385.1:p.Lys689Ter
ENST00000636227.1:n.3576A>T
ENST00000636254.1:n.1033A>T
ENST00000636930.2:c.5113A>T MANE Select	ENSP00000490491.2:p.Lys1705Ter
ENST00000636940.1:n.3110A>T
ENST00000637015.1:c.2481A>T
ENST00000637568.1:c.2395A>T
ENST00000637741.1:n.1779A>T
ENST00000637810.1:c.2455A>T	ENSP00000489636.1:p.Lys819Ter
ENST00000637904.1:c.2614A>T	ENSP00000490550.1:p.Lys872Ter
ENST00000647938.1:c.4744A>T	ENSP00000498155.1:p.Lys1582Ter
ENST00000346085.9:c.4744A>T	ENSP00000344546.4:p.Lys1582Ter
ENST00000350026.9:c.4705A>T	ENSP00000055163.7:p.Lys1569Ter
ENST00000414678.6:c.3271A>T	ENSP00000412835.2:p.Lys1091Ter
NM_017519.2:c.4705A>T	NP_059989.2:p.Lys1569Ter
NM_020732.3:c.4744A>T	NP_065783.3:p.Lys1582Ter
XM_005267069.3:c.4864A>T	XP_005267126.2:p.Lys1622Ter
XM_011535984.1:c.3943A>T	XP_011534286.1:p.Lys1315Ter
XM_011535985.1:c.3763A>T	XP_011534287.1:p.Lys1255Ter
XM_011535986.1:c.3523A>T	XP_011534288.1:p.Lys1175Ter
XM_011535987.1:c.3142A>T	XP_011534289.1:p.Lys1048Ter
XM_011535988.1:c.2005A>T	XP_011534290.1:p.Lys669Ter
NM_001346813.1:c.4864A>T	NP_001333742.1:p.Lys1622Ter
NM_001363725.1:c.2614A>T	NP_001350654.1:p.Lys872Ter
XM_011535984.2:c.5074A>T	XP_011534286.2:p.Lys1692Ter
XM_011535988.3:c.2005A>T	XP_011534290.1:p.Lys669Ter
XM_017011103.2:c.4975A>T	XP_016866592.1:p.Lys1659Ter
XM_017011104.1:c.4945A>T	XP_016866593.1:p.Lys1649Ter
XM_017011105.2:c.4915A>T	XP_016866594.1:p.Lys1639Ter
XM_017011106.2:c.4786A>T	XP_016866595.1:p.Lys1596Ter
XM_017011107.2:c.4765A>T	XP_016866596.1:p.Lys1589Ter
XR_002956289.1:n.5060A>T
NM_001363725.2:c.2614A>T	NP_001350654.1:p.Lys872Ter
NM_001371656.1:c.4993A>T	NP_001358585.1:p.Lys1665Ter
NM_001374820.1:c.4993A>T	NP_001361749.1:p.Lys1665Ter
NM_001374828.1:c.5113A>T MANE Select	NP_001361757.1:p.Lys1705Ter
NM_017519.3:c.4954A>T	NP_059989.3:p.Lys1652Ter