Canonical Allele Identifier: CA366238078

Gene: ARID1B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157196200C>T , CM000668.2:g.157196200C>T	GRCh38
NC_000006.11:g.157517334C>T , CM000668.1:g.157517334C>T	GRCh37
NC_000006.10:g.157559026C>T	NCBI36
NG_032093.1:g.423271C>T
NG_032093.2:g.423271C>T
NG_066624.1:g.425175C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001374828.1:c.4267C>T MANE Select	NP_001361757.1:p.Gln1423Ter
ENST00000636930.2:c.4267C>T MANE Select	ENSP00000490491.2:p.Gln1423Ter
NM_001346813.1:c.4018C>T	NP_001333742.1:p.Gln1340Ter
NM_001363725.1:c.1768C>T	NP_001350654.1:p.Gln590Ter
NM_001363725.2:c.1768C>T	NP_001350654.1:p.Gln590Ter
NM_001371656.1:c.4147C>T	NP_001358585.1:p.Gln1383Ter
NM_001374820.1:c.4147C>T	NP_001361749.1:p.Gln1383Ter
NM_017519.2:c.3859C>T	NP_059989.2:p.Gln1287Ter
NM_017519.3:c.4108C>T	NP_059989.3:p.Gln1370Ter
NM_020732.3:c.3898C>T	NP_065783.3:p.Gln1300Ter
ENST00000346085.10:c.4147C>T	ENSP00000344546.5:p.Gln1383Ter
ENST00000346085.9:c.3898C>T	ENSP00000344546.4:p.Gln1300Ter
ENST00000350026.10:c.3859C>T	ENSP00000055163.7:p.Gln1287Ter
ENST00000350026.11:c.4108C>T	ENSP00000055163.8:p.Gln1370Ter
ENST00000350026.9:c.3859C>T	ENSP00000055163.7:p.Gln1287Ter
ENST00000414678.6:c.2425C>T	ENSP00000412835.2:p.Gln809Ter
ENST00000414678.7:c.2425C>T	ENSP00000412835.2:p.Gln809Ter
ENST00000414678.8:c.4177C>T	ENSP00000412835.3:p.Gln1393Ter
ENST00000635849.1:c.1588C>T	ENSP00000490948.1:p.Gln530Ter
ENST00000635957.1:c.1219C>T	ENSP00000490385.1:p.Gln407Ter
ENST00000636227.1:n.2730C>T
ENST00000636940.1:n.2264C>T
ENST00000637015.1:c.1635C>T
ENST00000637015.2:c.4396C>T	ENSP00000489729.2:p.Gln1466Ter
ENST00000637568.1:c.1549C>T
ENST00000637741.1:n.933C>T
ENST00000637810.1:c.1609C>T	ENSP00000489636.1:p.Gln537Ter
ENST00000637904.1:c.1768C>T	ENSP00000490550.1:p.Gln590Ter
ENST00000647938.1:c.3898C>T	ENSP00000498155.1:p.Gln1300Ter
XM_005267069.3:c.4018C>T	XP_005267126.2:p.Gln1340Ter
XM_011535984.1:c.3097C>T	XP_011534286.1:p.Gln1033Ter
XM_011535984.2:c.4228C>T	XP_011534286.2:p.Gln1410Ter
XM_011535985.1:c.2917C>T	XP_011534287.1:p.Gln973Ter
XM_011535986.1:c.2677C>T	XP_011534288.1:p.Gln893Ter
XM_011535987.1:c.2296C>T	XP_011534289.1:p.Gln766Ter
XM_011535988.1:c.1159C>T	XP_011534290.1:p.Gln387Ter
XM_011535988.3:c.1159C>T	XP_011534290.1:p.Gln387Ter
XM_017011103.2:c.4129C>T	XP_016866592.1:p.Gln1377Ter
XM_017011104.1:c.4099C>T	XP_016866593.1:p.Gln1367Ter
XM_017011105.2:c.4069C>T	XP_016866594.1:p.Gln1357Ter
XM_017011106.2:c.3940C>T	XP_016866595.1:p.Gln1314Ter
XM_017011107.2:c.3919C>T	XP_016866596.1:p.Gln1307Ter
XR_002956289.1:n.4311C>T