Canonical Allele Identifier: CA366242453

Gene: ARID1B

Linked Data

• dbSNP Id: rs1562346715
• MyVariant Identifiers: chr6:g.157522441G>C (hg19) ; chr6:g.157201307G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201307G>C , CM000668.2:g.157201307G>C	GRCh38
NC_000006.11:g.157522441G>C , CM000668.1:g.157522441G>C	GRCh37
NC_000006.10:g.157564133G>C	NCBI36
NG_032093.1:g.428378G>C
NG_032093.2:g.428378G>C
NG_066624.1:g.430282G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4923G>C	ENSP00000055163.8:p.Lys1641Asn
ENST00000414678.8:c.4992G>C	ENSP00000412835.3:p.Lys1664Asn
ENST00000637015.2:c.5211G>C	ENSP00000489729.2:p.Lys1737Asn
ENST00000346085.10:c.4962G>C	ENSP00000344546.5:p.Lys1654Asn
ENST00000350026.10:c.4674G>C	ENSP00000055163.7:p.Lys1558Asn
ENST00000414678.7:c.3240G>C	ENSP00000412835.2:p.Lys1080Asn
ENST00000635849.1:c.2403G>C	ENSP00000490948.1:p.Lys801Asn
ENST00000635957.1:c.2034G>C	ENSP00000490385.1:p.Lys678Asn
ENST00000636227.1:n.3545G>C
ENST00000636254.1:n.1002G>C
ENST00000636930.2:c.5082G>C MANE Select	ENSP00000490491.2:p.Lys1694Asn
ENST00000636940.1:n.3079G>C
ENST00000637015.1:c.2450G>C
ENST00000637568.1:c.2364G>C
ENST00000637741.1:n.1748G>C
ENST00000637810.1:c.2424G>C	ENSP00000489636.1:p.Lys808Asn
ENST00000637904.1:c.2583G>C	ENSP00000490550.1:p.Lys861Asn
ENST00000647938.1:c.4713G>C	ENSP00000498155.1:p.Lys1571Asn
ENST00000346085.9:c.4713G>C	ENSP00000344546.4:p.Lys1571Asn
ENST00000350026.9:c.4674G>C	ENSP00000055163.7:p.Lys1558Asn
ENST00000414678.6:c.3240G>C	ENSP00000412835.2:p.Lys1080Asn
NM_017519.2:c.4674G>C	NP_059989.2:p.Lys1558Asn
NM_020732.3:c.4713G>C	NP_065783.3:p.Lys1571Asn
XM_005267069.3:c.4833G>C	XP_005267126.2:p.Lys1611Asn
XM_011535984.1:c.3912G>C	XP_011534286.1:p.Lys1304Asn
XM_011535985.1:c.3732G>C	XP_011534287.1:p.Lys1244Asn
XM_011535986.1:c.3492G>C	XP_011534288.1:p.Lys1164Asn
XM_011535987.1:c.3111G>C	XP_011534289.1:p.Lys1037Asn
XM_011535988.1:c.1974G>C	XP_011534290.1:p.Lys658Asn
NM_001346813.1:c.4833G>C	NP_001333742.1:p.Lys1611Asn
NM_001363725.1:c.2583G>C	NP_001350654.1:p.Lys861Asn
XM_011535984.2:c.5043G>C	XP_011534286.2:p.Lys1681Asn
XM_011535988.3:c.1974G>C	XP_011534290.1:p.Lys658Asn
XM_017011103.2:c.4944G>C	XP_016866592.1:p.Lys1648Asn
XM_017011104.1:c.4914G>C	XP_016866593.1:p.Lys1638Asn
XM_017011105.2:c.4884G>C	XP_016866594.1:p.Lys1628Asn
XM_017011106.2:c.4755G>C	XP_016866595.1:p.Lys1585Asn
XM_017011107.2:c.4734G>C	XP_016866596.1:p.Lys1578Asn
XR_002956289.1:n.5029G>C
NM_001363725.2:c.2583G>C	NP_001350654.1:p.Lys861Asn
NM_001371656.1:c.4962G>C	NP_001358585.1:p.Lys1654Asn
NM_001374820.1:c.4962G>C	NP_001361749.1:p.Lys1654Asn
NM_001374828.1:c.5082G>C MANE Select	NP_001361757.1:p.Lys1694Asn
NM_017519.3:c.4923G>C	NP_059989.3:p.Lys1641Asn