Canonical Allele Identifier: CA366235242

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511232A>C (hg19) ; chr6:g.157190098A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190098A>C , CM000668.2:g.157190098A>C	GRCh38
NC_000006.11:g.157511232A>C , CM000668.1:g.157511232A>C	GRCh37
NC_000006.10:g.157552924A>C	NCBI36
NG_032093.1:g.417169A>C
NG_032093.2:g.417169A>C
NG_066624.1:g.419073A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3960A>C	ENSP00000055163.8:p.Lys1320Asn
ENST00000414678.8:c.4029A>C	ENSP00000412835.3:p.Lys1343Asn
ENST00000637015.2:c.4248A>C	ENSP00000489729.2:p.Lys1416Asn
ENST00000346085.10:c.3999A>C	ENSP00000344546.5:p.Lys1333Asn
ENST00000350026.10:c.3711A>C	ENSP00000055163.7:p.Lys1237Asn
ENST00000414678.7:c.2277A>C	ENSP00000412835.2:p.Lys759Asn
ENST00000635849.1:c.1440A>C	ENSP00000490948.1:p.Lys480Asn
ENST00000635957.1:c.1071A>C	ENSP00000490385.1:p.Lys357Asn
ENST00000636930.2:c.4119A>C MANE Select	ENSP00000490491.2:p.Lys1373Asn
ENST00000636940.1:n.2116A>C
ENST00000637015.1:c.1487A>C
ENST00000637568.1:c.1401A>C
ENST00000637741.1:n.785A>C
ENST00000637810.1:c.1461A>C	ENSP00000489636.1:p.Lys487Asn
ENST00000637904.1:c.1620A>C	ENSP00000490550.1:p.Lys540Asn
ENST00000647938.1:c.3750A>C	ENSP00000498155.1:p.Lys1250Asn
ENST00000346085.9:c.3750A>C	ENSP00000344546.4:p.Lys1250Asn
ENST00000350026.9:c.3711A>C	ENSP00000055163.7:p.Lys1237Asn
ENST00000414678.6:c.2277A>C	ENSP00000412835.2:p.Lys759Asn
NM_017519.2:c.3711A>C	NP_059989.2:p.Lys1237Asn
NM_020732.3:c.3750A>C	NP_065783.3:p.Lys1250Asn
XM_005267069.3:c.3870A>C	XP_005267126.2:p.Lys1290Asn
XM_011535984.1:c.2949A>C	XP_011534286.1:p.Lys983Asn
XM_011535985.1:c.2769A>C	XP_011534287.1:p.Lys923Asn
XM_011535986.1:c.2529A>C	XP_011534288.1:p.Lys843Asn
XM_011535987.1:c.2148A>C	XP_011534289.1:p.Lys716Asn
XM_011535988.1:c.1011A>C	XP_011534290.1:p.Lys337Asn
NM_001346813.1:c.3870A>C	NP_001333742.1:p.Lys1290Asn
NM_001363725.1:c.1620A>C	NP_001350654.1:p.Lys540Asn
XM_011535984.2:c.4080A>C	XP_011534286.2:p.Lys1360Asn
XM_011535988.3:c.1011A>C	XP_011534290.1:p.Lys337Asn
XM_017011103.2:c.3981A>C	XP_016866592.1:p.Lys1327Asn
XM_017011104.1:c.3951A>C	XP_016866593.1:p.Lys1317Asn
XM_017011105.2:c.3921A>C	XP_016866594.1:p.Lys1307Asn
XM_017011106.2:c.3792A>C	XP_016866595.1:p.Lys1264Asn
XM_017011107.2:c.3771A>C	XP_016866596.1:p.Lys1257Asn
XR_002956289.1:n.4163A>C
NM_001363725.2:c.1620A>C	NP_001350654.1:p.Lys540Asn
NM_001371656.1:c.3999A>C	NP_001358585.1:p.Lys1333Asn
NM_001374820.1:c.3999A>C	NP_001361749.1:p.Lys1333Asn
NM_001374828.1:c.4119A>C MANE Select	NP_001361757.1:p.Lys1373Asn
NM_017519.3:c.3960A>C	NP_059989.3:p.Lys1320Asn