Canonical Allele Identifier: CA366248842

Gene: ARID1B

Linked Data

• ClinVar Variation Id: 521375
• ClinVar RCV Id: RCV000624474 ; RCV001533061 ; RCV001807308
• dbSNP Id: rs1554238035
• MyVariant Identifiers: chr6:g.157528597C>T (hg19) ; chr6:g.157207463C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157207463C>T , CM000668.2:g.157207463C>T	GRCh38
NC_000006.11:g.157528597C>T , CM000668.1:g.157528597C>T	GRCh37
NC_000006.10:g.157570289C>T	NCBI36
NG_032093.1:g.434534C>T
NG_032093.2:g.434534C>T
NG_066624.1:g.436438C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.6532C>T	ENSP00000055163.8:p.Gln2178Ter
ENST00000414678.8:c.6601C>T	ENSP00000412835.3:p.Gln2201Ter
ENST00000637015.2:c.6820C>T	ENSP00000489729.2:p.Gln2274Ter
ENST00000346085.10:c.6571C>T	ENSP00000344546.5:p.Gln2191Ter
ENST00000350026.10:c.6283C>T	ENSP00000055163.7:p.Gln2095Ter
ENST00000414678.7:c.4849C>T	ENSP00000412835.2:p.Gln1617Ter
ENST00000635849.1:c.4012C>T	ENSP00000490948.1:p.Gln1338Ter
ENST00000635928.1:c.847C>T	ENSP00000489717.1:p.Gln283Ter
ENST00000635957.1:c.3643C>T	ENSP00000490385.1:p.Gln1215Ter
ENST00000636227.1:n.5154C>T
ENST00000636254.1:n.2611C>T
ENST00000636930.2:c.6691C>T MANE Select	ENSP00000490491.2:p.Gln2231Ter
ENST00000636940.1:n.4688C>T
ENST00000637015.1:c.4059C>T
ENST00000637568.1:c.3973C>T
ENST00000637741.1:n.3357C>T
ENST00000637810.1:c.4033C>T	ENSP00000489636.1:p.Gln1345Ter
ENST00000637904.1:c.4192C>T	ENSP00000490550.1:p.Gln1398Ter
ENST00000637933.1:n.3806C>T
ENST00000647938.1:c.6322C>T	ENSP00000498155.1:p.Gln2108Ter
ENST00000346085.9:c.6322C>T	ENSP00000344546.4:p.Gln2108Ter
ENST00000350026.9:c.6283C>T	ENSP00000055163.7:p.Gln2095Ter
ENST00000414678.6:c.4849C>T	ENSP00000412835.2:p.Gln1617Ter
NM_017519.2:c.6283C>T	NP_059989.2:p.Gln2095Ter
NM_020732.3:c.6322C>T	NP_065783.3:p.Gln2108Ter
XM_005267069.3:c.6442C>T	XP_005267126.2:p.Gln2148Ter
XM_011535984.1:c.5521C>T	XP_011534286.1:p.Gln1841Ter
XM_011535985.1:c.5341C>T	XP_011534287.1:p.Gln1781Ter
XM_011535986.1:c.5101C>T	XP_011534288.1:p.Gln1701Ter
XM_011535987.1:c.4720C>T	XP_011534289.1:p.Gln1574Ter
XM_011535988.1:c.3583C>T	XP_011534290.1:p.Gln1195Ter
NM_001346813.1:c.6442C>T	NP_001333742.1:p.Gln2148Ter
NM_001363725.1:c.4192C>T	NP_001350654.1:p.Gln1398Ter
XM_011535984.2:c.6652C>T	XP_011534286.2:p.Gln2218Ter
XM_011535988.3:c.3583C>T	XP_011534290.1:p.Gln1195Ter
XM_017011103.2:c.6553C>T	XP_016866592.1:p.Gln2185Ter
XM_017011104.1:c.6523C>T	XP_016866593.1:p.Gln2175Ter
XM_017011105.2:c.6493C>T	XP_016866594.1:p.Gln2165Ter
XM_017011106.2:c.6364C>T	XP_016866595.1:p.Gln2122Ter
XM_017011107.2:c.6343C>T	XP_016866596.1:p.Gln2115Ter
XR_002956289.1:n.6638C>T
NM_001363725.2:c.4192C>T	NP_001350654.1:p.Gln1398Ter
NM_001371656.1:c.6571C>T	NP_001358585.1:p.Gln2191Ter
NM_001374820.1:c.6571C>T	NP_001361749.1:p.Gln2191Ter
NM_001374828.1:c.6691C>T MANE Select	NP_001361757.1:p.Gln2231Ter
NM_017519.3:c.6532C>T	NP_059989.3:p.Gln2178Ter