Canonical Allele Identifier: CA366240916

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 1956405
• ClinVar RCV Id: RCV002700824
• dbSNP Id: rs1794042426
• MyVariant Identifiers: chr6:g.157521914T>C (hg19) ; chr6:g.157200780T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200780T>C , CM000668.2:g.157200780T>C	GRCh38
NC_000006.11:g.157521914T>C , CM000668.1:g.157521914T>C	GRCh37
NC_000006.10:g.157563606T>C	NCBI36
NG_032093.1:g.427851T>C
NG_032093.2:g.427851T>C
NG_066624.1:g.429755T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4396T>C	ENSP00000055163.8:p.Tyr1466His
ENST00000414678.8:c.4465T>C	ENSP00000412835.3:p.Tyr1489His
ENST00000637015.2:c.4684T>C	ENSP00000489729.2:p.Tyr1562His
ENST00000346085.10:c.4435T>C	ENSP00000344546.5:p.Tyr1479His
ENST00000350026.10:c.4147T>C	ENSP00000055163.7:p.Tyr1383His
ENST00000414678.7:c.2713T>C	ENSP00000412835.2:p.Tyr905His
ENST00000635849.1:c.1876T>C	ENSP00000490948.1:p.Tyr626His
ENST00000635957.1:c.1507T>C	ENSP00000490385.1:p.Tyr503His
ENST00000636227.1:n.3018T>C
ENST00000636254.1:n.475T>C
ENST00000636930.2:c.4555T>C MANE Select	ENSP00000490491.2:p.Tyr1519His
ENST00000636940.1:n.2552T>C
ENST00000637015.1:c.1923T>C
ENST00000637568.1:c.1837T>C
ENST00000637741.1:n.1221T>C
ENST00000637810.1:c.1897T>C	ENSP00000489636.1:p.Tyr633His
ENST00000637904.1:c.2056T>C	ENSP00000490550.1:p.Tyr686His
ENST00000647938.1:c.4186T>C	ENSP00000498155.1:p.Tyr1396His
ENST00000346085.9:c.4186T>C	ENSP00000344546.4:p.Tyr1396His
ENST00000350026.9:c.4147T>C	ENSP00000055163.7:p.Tyr1383His
ENST00000414678.6:c.2713T>C	ENSP00000412835.2:p.Tyr905His
NM_017519.2:c.4147T>C	NP_059989.2:p.Tyr1383His
NM_020732.3:c.4186T>C	NP_065783.3:p.Tyr1396His
XM_005267069.3:c.4306T>C	XP_005267126.2:p.Tyr1436His
XM_011535984.1:c.3385T>C	XP_011534286.1:p.Tyr1129His
XM_011535985.1:c.3205T>C	XP_011534287.1:p.Tyr1069His
XM_011535986.1:c.2965T>C	XP_011534288.1:p.Tyr989His
XM_011535987.1:c.2584T>C	XP_011534289.1:p.Tyr862His
XM_011535988.1:c.1447T>C	XP_011534290.1:p.Tyr483His
NM_001346813.1:c.4306T>C	NP_001333742.1:p.Tyr1436His
NM_001363725.1:c.2056T>C	NP_001350654.1:p.Tyr686His
XM_011535984.2:c.4516T>C	XP_011534286.2:p.Tyr1506His
XM_011535988.3:c.1447T>C	XP_011534290.1:p.Tyr483His
XM_017011103.2:c.4417T>C	XP_016866592.1:p.Tyr1473His
XM_017011104.1:c.4387T>C	XP_016866593.1:p.Tyr1463His
XM_017011105.2:c.4357T>C	XP_016866594.1:p.Tyr1453His
XM_017011106.2:c.4228T>C	XP_016866595.1:p.Tyr1410His
XM_017011107.2:c.4207T>C	XP_016866596.1:p.Tyr1403His
XR_002956289.1:n.4502T>C
NM_001363725.2:c.2056T>C	NP_001350654.1:p.Tyr686His
NM_001371656.1:c.4435T>C	NP_001358585.1:p.Tyr1479His
NM_001374820.1:c.4435T>C	NP_001361749.1:p.Tyr1479His
NM_001374828.1:c.4555T>C MANE Select	NP_001361757.1:p.Tyr1519His
NM_017519.3:c.4396T>C	NP_059989.3:p.Tyr1466His