Canonical Allele Identifier: CA366388699

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1309359
• ClinVar RCV Id: RCV001765528
• dbSNP Id: rs2128634027
• MyVariant Identifiers: chr6:g.157469803G>C (hg19) ; chr6:g.157148669G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148669G>C , CM000668.2:g.157148669G>C	GRCh38
NC_000006.11:g.157469803G>C , CM000668.1:g.157469803G>C	GRCh37
NC_000006.10:g.157511495G>C	NCBI36
NG_032093.1:g.375740G>C
NG_032093.2:g.375740G>C
NG_066624.1:g.377644G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2807G>C	ENSP00000055163.8:p.Ser936Thr
ENST00000414678.8:c.2717G>C	ENSP00000412835.3:p.Ser906Thr
ENST00000637015.2:c.2807G>C	ENSP00000489729.2:p.Ser936Thr
ENST00000319584.11:c.821G>C	ENSP00000313006.7:p.Ser274Thr
ENST00000346085.10:c.2846G>C	ENSP00000344546.5:p.Ser949Thr
ENST00000350026.10:c.2558G>C	ENSP00000055163.7:p.Ser853Thr
ENST00000414678.7:c.965G>C	ENSP00000412835.2:p.Ser322Thr
ENST00000452544.2:n.708G>C
ENST00000635849.1:c.128G>C	ENSP00000490948.1:p.Ser43Thr
ENST00000636930.2:c.2807G>C MANE Select	ENSP00000490491.2:p.Ser936Thr
ENST00000637015.1:c.46G>C
ENST00000637810.1:c.308G>C	ENSP00000489636.1:p.Ser103Thr
ENST00000637904.1:c.308G>C	ENSP00000490550.1:p.Ser103Thr
ENST00000647938.1:c.2597G>C	ENSP00000498155.1:p.Ser866Thr
ENST00000674190.1:n.1556G>C
ENST00000319584.10:c.824G>C	ENSP00000313006.6:p.Ser275Thr
ENST00000346085.9:c.2597G>C	ENSP00000344546.4:p.Ser866Thr
ENST00000350026.9:c.2558G>C	ENSP00000055163.7:p.Ser853Thr
ENST00000414678.6:c.965G>C	ENSP00000412835.2:p.Ser322Thr
ENST00000452544.1:n.654G>C
NM_017519.2:c.2558G>C	NP_059989.2:p.Ser853Thr
NM_020732.3:c.2597G>C	NP_065783.3:p.Ser866Thr
XM_005267069.3:c.2558G>C	XP_005267126.2:p.Ser853Thr
XM_011535984.1:c.1508G>C	XP_011534286.1:p.Ser503Thr
XM_011535985.1:c.1328G>C	XP_011534287.1:p.Ser443Thr
XM_011535986.1:c.1088G>C	XP_011534288.1:p.Ser363Thr
XM_011535987.1:c.707G>C	XP_011534289.1:p.Ser236Thr
XM_011535988.1:c.-20+15462G>C	XP_011534290.1:n.-20+15462G>C
NM_001346813.1:c.2558G>C	NP_001333742.1:p.Ser853Thr
NM_001363725.1:c.308G>C	NP_001350654.1:p.Ser103Thr
XM_011535984.2:c.2639G>C	XP_011534286.2:p.Ser880Thr
XM_011535988.3:c.-20+15462G>C	XP_011534290.1:n.-20+15462G>C
XM_017011103.2:c.2639G>C	XP_016866592.1:p.Ser880Thr
XM_017011104.1:c.2639G>C	XP_016866593.1:p.Ser880Thr
XM_017011105.2:c.2639G>C	XP_016866594.1:p.Ser880Thr
XM_017011106.2:c.2639G>C	XP_016866595.1:p.Ser880Thr
XM_017011107.2:c.2459G>C	XP_016866596.1:p.Ser820Thr
XR_002956289.1:n.2722G>C
NM_001363725.2:c.308G>C	NP_001350654.1:p.Ser103Thr
NM_001371656.1:c.2846G>C	NP_001358585.1:p.Ser949Thr
NM_001374820.1:c.2846G>C	NP_001361749.1:p.Ser949Thr
NM_001374828.1:c.2807G>C MANE Select	NP_001361757.1:p.Ser936Thr
NM_017519.3:c.2807G>C	NP_059989.3:p.Ser936Thr