Canonical Allele Identifier: CA366228165

Gene: ARID1B

Linked Data

• dbSNP Id: rs374705142
• MyVariant Identifiers: chr6:g.157502255G>C (hg19) ; chr6:g.157181121G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181121G>C , CM000668.2:g.157181121G>C	GRCh38
NC_000006.11:g.157502255G>C , CM000668.1:g.157502255G>C	GRCh37
NC_000006.10:g.157543947G>C	NCBI36
NG_032093.1:g.408192G>C
NG_032093.2:g.408192G>C
NG_066624.1:g.410096G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3498G>C	ENSP00000055163.8:p.Lys1166Asn
ENST00000414678.8:c.3567G>C	ENSP00000412835.3:p.Lys1189Asn
ENST00000637015.2:c.3786G>C	ENSP00000489729.2:p.Lys1262Asn
ENST00000319584.11:c.1671G>C	ENSP00000313006.7:p.Lys557Asn
ENST00000346085.10:c.3537G>C	ENSP00000344546.5:p.Lys1179Asn
ENST00000350026.10:c.3249G>C	ENSP00000055163.7:p.Lys1083Asn
ENST00000414678.7:c.1815G>C	ENSP00000412835.2:p.Lys605Asn
ENST00000635849.1:c.978G>C	ENSP00000490948.1:p.Lys326Asn
ENST00000635957.1:c.612G>C	ENSP00000490385.1:p.Lys204Asn
ENST00000636930.2:c.3657G>C MANE Select	ENSP00000490491.2:p.Lys1219Asn
ENST00000636940.1:n.1654G>C
ENST00000637015.1:c.1025G>C
ENST00000637568.1:c.939G>C
ENST00000637741.1:n.323G>C
ENST00000637810.1:c.999G>C	ENSP00000489636.1:p.Lys333Asn
ENST00000637904.1:c.1158G>C	ENSP00000490550.1:p.Lys386Asn
ENST00000647938.1:c.3288G>C	ENSP00000498155.1:p.Lys1096Asn
ENST00000319584.10:c.1674G>C	ENSP00000313006.6:p.Lys558Asn
ENST00000346085.9:c.3288G>C	ENSP00000344546.4:p.Lys1096Asn
ENST00000350026.9:c.3249G>C	ENSP00000055163.7:p.Lys1083Asn
ENST00000400790.3:c.450G>C	ENSP00000383596.3:p.Lys150Asn
ENST00000414678.6:c.1815G>C	ENSP00000412835.2:p.Lys605Asn
ENST00000478761.3:c.859G>C
NM_017519.2:c.3249G>C	NP_059989.2:p.Lys1083Asn
NM_020732.3:c.3288G>C	NP_065783.3:p.Lys1096Asn
XM_005267069.3:c.3408G>C	XP_005267126.2:p.Lys1136Asn
XM_011535984.1:c.2487G>C	XP_011534286.1:p.Lys829Asn
XM_011535985.1:c.2307G>C	XP_011534287.1:p.Lys769Asn
XM_011535986.1:c.2067G>C	XP_011534288.1:p.Lys689Asn
XM_011535987.1:c.1686G>C	XP_011534289.1:p.Lys562Asn
XM_011535988.1:c.549G>C	XP_011534290.1:p.Lys183Asn
NM_001346813.1:c.3408G>C	NP_001333742.1:p.Lys1136Asn
NM_001363725.1:c.1158G>C	NP_001350654.1:p.Lys386Asn
XM_011535984.2:c.3618G>C	XP_011534286.2:p.Lys1206Asn
XM_011535988.3:c.549G>C	XP_011534290.1:p.Lys183Asn
XM_017011103.2:c.3519G>C	XP_016866592.1:p.Lys1173Asn
XM_017011104.1:c.3489G>C	XP_016866593.1:p.Lys1163Asn
XM_017011105.2:c.3459G>C	XP_016866594.1:p.Lys1153Asn
XM_017011106.2:c.3330G>C	XP_016866595.1:p.Lys1110Asn
XM_017011107.2:c.3309G>C	XP_016866596.1:p.Lys1103Asn
XR_002956289.1:n.3701G>C
NM_001363725.2:c.1158G>C	NP_001350654.1:p.Lys386Asn
NM_001371656.1:c.3537G>C	NP_001358585.1:p.Lys1179Asn
NM_001374820.1:c.3537G>C	NP_001361749.1:p.Lys1179Asn
NM_001374828.1:c.3657G>C MANE Select	NP_001361757.1:p.Lys1219Asn
NM_017519.3:c.3498G>C	NP_059989.3:p.Lys1166Asn