Canonical Allele Identifier: CA16605005

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 386900
• ClinVar RCV Id: RCV000443436
• dbSNP Id: rs1057522635
• MyVariant Identifiers: chr6:g.157511230A>C (hg19) ; chr6:g.157190096A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190096A>C , CM000668.2:g.157190096A>C	GRCh38
NC_000006.11:g.157511230A>C , CM000668.1:g.157511230A>C	GRCh37
NC_000006.10:g.157552922A>C	NCBI36
NG_032093.1:g.417167A>C
NG_032093.2:g.417167A>C
NG_066624.1:g.419071A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3958A>C	ENSP00000055163.8:p.Lys1320Gln
ENST00000414678.8:c.4027A>C	ENSP00000412835.3:p.Lys1343Gln
ENST00000637015.2:c.4246A>C	ENSP00000489729.2:p.Lys1416Gln
ENST00000346085.10:c.3997A>C	ENSP00000344546.5:p.Lys1333Gln
ENST00000350026.10:c.3709A>C	ENSP00000055163.7:p.Lys1237Gln
ENST00000414678.7:c.2275A>C	ENSP00000412835.2:p.Lys759Gln
ENST00000635849.1:c.1438A>C	ENSP00000490948.1:p.Lys480Gln
ENST00000635957.1:c.1069A>C	ENSP00000490385.1:p.Lys357Gln
ENST00000636930.2:c.4117A>C MANE Select	ENSP00000490491.2:p.Lys1373Gln
ENST00000636940.1:n.2114A>C
ENST00000637015.1:c.1485A>C
ENST00000637568.1:c.1399A>C
ENST00000637741.1:n.783A>C
ENST00000637810.1:c.1459A>C	ENSP00000489636.1:p.Lys487Gln
ENST00000637904.1:c.1618A>C	ENSP00000490550.1:p.Lys540Gln
ENST00000647938.1:c.3748A>C	ENSP00000498155.1:p.Lys1250Gln
ENST00000346085.9:c.3748A>C	ENSP00000344546.4:p.Lys1250Gln
ENST00000350026.9:c.3709A>C	ENSP00000055163.7:p.Lys1237Gln
ENST00000414678.6:c.2275A>C	ENSP00000412835.2:p.Lys759Gln
NM_017519.2:c.3709A>C	NP_059989.2:p.Lys1237Gln
NM_020732.3:c.3748A>C	NP_065783.3:p.Lys1250Gln
XM_005267069.3:c.3868A>C	XP_005267126.2:p.Lys1290Gln
XM_011535984.1:c.2947A>C	XP_011534286.1:p.Lys983Gln
XM_011535985.1:c.2767A>C	XP_011534287.1:p.Lys923Gln
XM_011535986.1:c.2527A>C	XP_011534288.1:p.Lys843Gln
XM_011535987.1:c.2146A>C	XP_011534289.1:p.Lys716Gln
XM_011535988.1:c.1009A>C	XP_011534290.1:p.Lys337Gln
NM_001346813.1:c.3868A>C	NP_001333742.1:p.Lys1290Gln
NM_001363725.1:c.1618A>C	NP_001350654.1:p.Lys540Gln
XM_011535984.2:c.4078A>C	XP_011534286.2:p.Lys1360Gln
XM_011535988.3:c.1009A>C	XP_011534290.1:p.Lys337Gln
XM_017011103.2:c.3979A>C	XP_016866592.1:p.Lys1327Gln
XM_017011104.1:c.3949A>C	XP_016866593.1:p.Lys1317Gln
XM_017011105.2:c.3919A>C	XP_016866594.1:p.Lys1307Gln
XM_017011106.2:c.3790A>C	XP_016866595.1:p.Lys1264Gln
XM_017011107.2:c.3769A>C	XP_016866596.1:p.Lys1257Gln
XR_002956289.1:n.4161A>C
NM_001363725.2:c.1618A>C	NP_001350654.1:p.Lys540Gln
NM_001371656.1:c.3997A>C	NP_001358585.1:p.Lys1333Gln
NM_001374820.1:c.3997A>C	NP_001361749.1:p.Lys1333Gln
NM_001374828.1:c.4117A>C MANE Select	NP_001361757.1:p.Lys1373Gln
NM_017519.3:c.3958A>C	NP_059989.3:p.Lys1320Gln