Canonical Allele Identifier: CA452990142

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470074A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148940A>C , CM000668.2:g.157148940A>C	GRCh38
NC_000006.11:g.157470074A>C , CM000668.1:g.157470074A>C	GRCh37
NC_000006.10:g.157511766A>C	NCBI36
NG_032093.1:g.376011A>C
NG_032093.2:g.376011A>C
NG_066624.1:g.377915A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3078A>C	ENSP00000055163.8:p.Ser1026=
ENST00000414678.8:c.2988A>C	ENSP00000412835.3:p.Ser996=
ENST00000637015.2:c.3078A>C	ENSP00000489729.2:p.Ser1026=
ENST00000319584.11:c.1092A>C	ENSP00000313006.7:p.Ser364=
ENST00000346085.10:c.3117A>C	ENSP00000344546.5:p.Ser1039=
ENST00000350026.10:c.2829A>C	ENSP00000055163.7:p.Ser943=
ENST00000414678.7:c.1236A>C	ENSP00000412835.2:p.Ser412=
ENST00000452544.2:n.979A>C
ENST00000635849.1:c.399A>C	ENSP00000490948.1:p.Ser133=
ENST00000635957.1:c.33A>C	ENSP00000490385.1:p.Ser11=
ENST00000636426.1:n.212A>C
ENST00000636930.2:c.3078A>C MANE Select	ENSP00000490491.2:p.Ser1026=
ENST00000637015.1:c.317A>C
ENST00000637568.1:c.121A>C
ENST00000637810.1:c.579A>C	ENSP00000489636.1:p.Ser193=
ENST00000637904.1:c.579A>C	ENSP00000490550.1:p.Ser193=
ENST00000647938.1:c.2868A>C	ENSP00000498155.1:p.Ser956=
ENST00000674190.1:n.1827A>C
ENST00000319584.10:c.1095A>C	ENSP00000313006.6:p.Ser365=
ENST00000346085.9:c.2868A>C	ENSP00000344546.4:p.Ser956=
ENST00000350026.9:c.2829A>C	ENSP00000055163.7:p.Ser943=
ENST00000400790.3:c.30A>C	ENSP00000383596.3:p.Ser10=
ENST00000414678.6:c.1236A>C	ENSP00000412835.2:p.Ser412=
ENST00000452544.1:n.925A>C
ENST00000478761.3:c.151A>C
NM_017519.2:c.2829A>C	NP_059989.2:p.Ser943=
NM_020732.3:c.2868A>C	NP_065783.3:p.Ser956=
XM_005267069.3:c.2829A>C	XP_005267126.2:p.Ser943=
XM_011535984.1:c.1779A>C	XP_011534286.1:p.Ser593=
XM_011535985.1:c.1599A>C	XP_011534287.1:p.Ser533=
XM_011535986.1:c.1359A>C	XP_011534288.1:p.Ser453=
XM_011535987.1:c.978A>C	XP_011534289.1:p.Ser326=
XM_011535988.1:c.-20+15733A>C	XP_011534290.1:n.-20+15733A>C
NM_001346813.1:c.2829A>C	NP_001333742.1:p.Ser943=
NM_001363725.1:c.579A>C	NP_001350654.1:p.Ser193=
XM_011535984.2:c.2910A>C	XP_011534286.2:p.Ser970=
XM_011535988.3:c.-20+15733A>C	XP_011534290.1:n.-20+15733A>C
XM_017011103.2:c.2910A>C	XP_016866592.1:p.Ser970=
XM_017011104.1:c.2910A>C	XP_016866593.1:p.Ser970=
XM_017011105.2:c.2910A>C	XP_016866594.1:p.Ser970=
XM_017011106.2:c.2910A>C	XP_016866595.1:p.Ser970=
XM_017011107.2:c.2730A>C	XP_016866596.1:p.Ser910=
XR_002956289.1:n.2993A>C
NM_001363725.2:c.579A>C	NP_001350654.1:p.Ser193=
NM_001371656.1:c.3117A>C	NP_001358585.1:p.Ser1039=
NM_001374820.1:c.3117A>C	NP_001361749.1:p.Ser1039=
NM_001374828.1:c.3078A>C MANE Select	NP_001361757.1:p.Ser1026=
NM_017519.3:c.3078A>C	NP_059989.3:p.Ser1026=