Canonical Allele Identifier: CA366228415

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157502291A>C (hg19) ; chr6:g.157181157A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157181157A>C , CM000668.2:g.157181157A>C	GRCh38
NC_000006.11:g.157502291A>C , CM000668.1:g.157502291A>C	GRCh37
NC_000006.10:g.157543983A>C	NCBI36
NG_032093.1:g.408228A>C
NG_032093.2:g.408228A>C
NG_066624.1:g.410132A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3534A>C	ENSP00000055163.8:p.Lys1178Asn
ENST00000414678.8:c.3603A>C	ENSP00000412835.3:p.Lys1201Asn
ENST00000637015.2:c.3822A>C	ENSP00000489729.2:p.Lys1274Asn
ENST00000319584.11:c.1707A>C	ENSP00000313006.7:p.Lys569Asn
ENST00000346085.10:c.3573A>C	ENSP00000344546.5:p.Lys1191Asn
ENST00000350026.10:c.3285A>C	ENSP00000055163.7:p.Lys1095Asn
ENST00000414678.7:c.1851A>C	ENSP00000412835.2:p.Lys617Asn
ENST00000635849.1:c.1014A>C	ENSP00000490948.1:p.Lys338Asn
ENST00000635957.1:c.648A>C	ENSP00000490385.1:p.Lys216Asn
ENST00000636930.2:c.3693A>C MANE Select	ENSP00000490491.2:p.Lys1231Asn
ENST00000636940.1:n.1690A>C
ENST00000637015.1:c.1061A>C
ENST00000637568.1:c.975A>C
ENST00000637741.1:n.359A>C
ENST00000637810.1:c.1035A>C	ENSP00000489636.1:p.Lys345Asn
ENST00000637904.1:c.1194A>C	ENSP00000490550.1:p.Lys398Asn
ENST00000647938.1:c.3324A>C	ENSP00000498155.1:p.Lys1108Asn
ENST00000319584.10:c.1710A>C	ENSP00000313006.6:p.Lys570Asn
ENST00000346085.9:c.3324A>C	ENSP00000344546.4:p.Lys1108Asn
ENST00000350026.9:c.3285A>C	ENSP00000055163.7:p.Lys1095Asn
ENST00000400790.3:c.486A>C	ENSP00000383596.3:p.Lys162Asn
ENST00000414678.6:c.1851A>C	ENSP00000412835.2:p.Lys617Asn
ENST00000478761.3:c.895A>C
NM_017519.2:c.3285A>C	NP_059989.2:p.Lys1095Asn
NM_020732.3:c.3324A>C	NP_065783.3:p.Lys1108Asn
XM_005267069.3:c.3444A>C	XP_005267126.2:p.Lys1148Asn
XM_011535984.1:c.2523A>C	XP_011534286.1:p.Lys841Asn
XM_011535985.1:c.2343A>C	XP_011534287.1:p.Lys781Asn
XM_011535986.1:c.2103A>C	XP_011534288.1:p.Lys701Asn
XM_011535987.1:c.1722A>C	XP_011534289.1:p.Lys574Asn
XM_011535988.1:c.585A>C	XP_011534290.1:p.Lys195Asn
NM_001346813.1:c.3444A>C	NP_001333742.1:p.Lys1148Asn
NM_001363725.1:c.1194A>C	NP_001350654.1:p.Lys398Asn
XM_011535984.2:c.3654A>C	XP_011534286.2:p.Lys1218Asn
XM_011535988.3:c.585A>C	XP_011534290.1:p.Lys195Asn
XM_017011103.2:c.3555A>C	XP_016866592.1:p.Lys1185Asn
XM_017011104.1:c.3525A>C	XP_016866593.1:p.Lys1175Asn
XM_017011105.2:c.3495A>C	XP_016866594.1:p.Lys1165Asn
XM_017011106.2:c.3366A>C	XP_016866595.1:p.Lys1122Asn
XM_017011107.2:c.3345A>C	XP_016866596.1:p.Lys1115Asn
XR_002956289.1:n.3737A>C
NM_001363725.2:c.1194A>C	NP_001350654.1:p.Lys398Asn
NM_001371656.1:c.3573A>C	NP_001358585.1:p.Lys1191Asn
NM_001374820.1:c.3573A>C	NP_001361749.1:p.Lys1191Asn
NM_001374828.1:c.3693A>C MANE Select	NP_001361757.1:p.Lys1231Asn
NM_017519.3:c.3534A>C	NP_059989.3:p.Lys1178Asn