Canonical Allele Identifier: CA366228407

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502290A>C (hg19) ; chr6:g.157181156A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181156A>C , CM000668.2:g.157181156A>C	GRCh38
NC_000006.11:g.157502290A>C , CM000668.1:g.157502290A>C	GRCh37
NC_000006.10:g.157543982A>C	NCBI36
NG_032093.1:g.408227A>C
NG_032093.2:g.408227A>C
NG_066624.1:g.410131A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3533A>C	ENSP00000055163.8:p.Lys1178Thr
ENST00000414678.8:c.3602A>C	ENSP00000412835.3:p.Lys1201Thr
ENST00000637015.2:c.3821A>C	ENSP00000489729.2:p.Lys1274Thr
ENST00000319584.11:c.1706A>C	ENSP00000313006.7:p.Lys569Thr
ENST00000346085.10:c.3572A>C	ENSP00000344546.5:p.Lys1191Thr
ENST00000350026.10:c.3284A>C	ENSP00000055163.7:p.Lys1095Thr
ENST00000414678.7:c.1850A>C	ENSP00000412835.2:p.Lys617Thr
ENST00000635849.1:c.1013A>C	ENSP00000490948.1:p.Lys338Thr
ENST00000635957.1:c.647A>C	ENSP00000490385.1:p.Lys216Thr
ENST00000636930.2:c.3692A>C MANE Select	ENSP00000490491.2:p.Lys1231Thr
ENST00000636940.1:n.1689A>C
ENST00000637015.1:c.1060A>C
ENST00000637568.1:c.974A>C
ENST00000637741.1:n.358A>C
ENST00000637810.1:c.1034A>C	ENSP00000489636.1:p.Lys345Thr
ENST00000637904.1:c.1193A>C	ENSP00000490550.1:p.Lys398Thr
ENST00000647938.1:c.3323A>C	ENSP00000498155.1:p.Lys1108Thr
ENST00000319584.10:c.1709A>C	ENSP00000313006.6:p.Lys570Thr
ENST00000346085.9:c.3323A>C	ENSP00000344546.4:p.Lys1108Thr
ENST00000350026.9:c.3284A>C	ENSP00000055163.7:p.Lys1095Thr
ENST00000400790.3:c.485A>C	ENSP00000383596.3:p.Lys162Thr
ENST00000414678.6:c.1850A>C	ENSP00000412835.2:p.Lys617Thr
ENST00000478761.3:c.894A>C
NM_017519.2:c.3284A>C	NP_059989.2:p.Lys1095Thr
NM_020732.3:c.3323A>C	NP_065783.3:p.Lys1108Thr
XM_005267069.3:c.3443A>C	XP_005267126.2:p.Lys1148Thr
XM_011535984.1:c.2522A>C	XP_011534286.1:p.Lys841Thr
XM_011535985.1:c.2342A>C	XP_011534287.1:p.Lys781Thr
XM_011535986.1:c.2102A>C	XP_011534288.1:p.Lys701Thr
XM_011535987.1:c.1721A>C	XP_011534289.1:p.Lys574Thr
XM_011535988.1:c.584A>C	XP_011534290.1:p.Lys195Thr
NM_001346813.1:c.3443A>C	NP_001333742.1:p.Lys1148Thr
NM_001363725.1:c.1193A>C	NP_001350654.1:p.Lys398Thr
XM_011535984.2:c.3653A>C	XP_011534286.2:p.Lys1218Thr
XM_011535988.3:c.584A>C	XP_011534290.1:p.Lys195Thr
XM_017011103.2:c.3554A>C	XP_016866592.1:p.Lys1185Thr
XM_017011104.1:c.3524A>C	XP_016866593.1:p.Lys1175Thr
XM_017011105.2:c.3494A>C	XP_016866594.1:p.Lys1165Thr
XM_017011106.2:c.3365A>C	XP_016866595.1:p.Lys1122Thr
XM_017011107.2:c.3344A>C	XP_016866596.1:p.Lys1115Thr
XR_002956289.1:n.3736A>C
NM_001363725.2:c.1193A>C	NP_001350654.1:p.Lys398Thr
NM_001371656.1:c.3572A>C	NP_001358585.1:p.Lys1191Thr
NM_001374820.1:c.3572A>C	NP_001361749.1:p.Lys1191Thr
NM_001374828.1:c.3692A>C MANE Select	NP_001361757.1:p.Lys1231Thr
NM_017519.3:c.3533A>C	NP_059989.3:p.Lys1178Thr