Canonical Allele Identifier: CA366241838

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522208A>C (hg19) ; chr6:g.157201074A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201074A>C , CM000668.2:g.157201074A>C	GRCh38
NC_000006.11:g.157522208A>C , CM000668.1:g.157522208A>C	GRCh37
NC_000006.10:g.157563900A>C	NCBI36
NG_032093.1:g.428145A>C
NG_032093.2:g.428145A>C
NG_066624.1:g.430049A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4690A>C	ENSP00000055163.8:p.Asn1564His
ENST00000414678.8:c.4759A>C	ENSP00000412835.3:p.Asn1587His
ENST00000637015.2:c.4978A>C	ENSP00000489729.2:p.Asn1660His
ENST00000346085.10:c.4729A>C	ENSP00000344546.5:p.Asn1577His
ENST00000350026.10:c.4441A>C	ENSP00000055163.7:p.Asn1481His
ENST00000414678.7:c.3007A>C	ENSP00000412835.2:p.Asn1003His
ENST00000635849.1:c.2170A>C	ENSP00000490948.1:p.Asn724His
ENST00000635957.1:c.1801A>C	ENSP00000490385.1:p.Asn601His
ENST00000636227.1:n.3312A>C
ENST00000636254.1:n.769A>C
ENST00000636930.2:c.4849A>C MANE Select	ENSP00000490491.2:p.Asn1617His
ENST00000636940.1:n.2846A>C
ENST00000637015.1:c.2217A>C
ENST00000637568.1:c.2131A>C
ENST00000637741.1:n.1515A>C
ENST00000637810.1:c.2191A>C	ENSP00000489636.1:p.Asn731His
ENST00000637904.1:c.2350A>C	ENSP00000490550.1:p.Asn784His
ENST00000647938.1:c.4480A>C	ENSP00000498155.1:p.Asn1494His
ENST00000346085.9:c.4480A>C	ENSP00000344546.4:p.Asn1494His
ENST00000350026.9:c.4441A>C	ENSP00000055163.7:p.Asn1481His
ENST00000414678.6:c.3007A>C	ENSP00000412835.2:p.Asn1003His
NM_017519.2:c.4441A>C	NP_059989.2:p.Asn1481His
NM_020732.3:c.4480A>C	NP_065783.3:p.Asn1494His
XM_005267069.3:c.4600A>C	XP_005267126.2:p.Asn1534His
XM_011535984.1:c.3679A>C	XP_011534286.1:p.Asn1227His
XM_011535985.1:c.3499A>C	XP_011534287.1:p.Asn1167His
XM_011535986.1:c.3259A>C	XP_011534288.1:p.Asn1087His
XM_011535987.1:c.2878A>C	XP_011534289.1:p.Asn960His
XM_011535988.1:c.1741A>C	XP_011534290.1:p.Asn581His
NM_001346813.1:c.4600A>C	NP_001333742.1:p.Asn1534His
NM_001363725.1:c.2350A>C	NP_001350654.1:p.Asn784His
XM_011535984.2:c.4810A>C	XP_011534286.2:p.Asn1604His
XM_011535988.3:c.1741A>C	XP_011534290.1:p.Asn581His
XM_017011103.2:c.4711A>C	XP_016866592.1:p.Asn1571His
XM_017011104.1:c.4681A>C	XP_016866593.1:p.Asn1561His
XM_017011105.2:c.4651A>C	XP_016866594.1:p.Asn1551His
XM_017011106.2:c.4522A>C	XP_016866595.1:p.Asn1508His
XM_017011107.2:c.4501A>C	XP_016866596.1:p.Asn1501His
XR_002956289.1:n.4796A>C
NM_001363725.2:c.2350A>C	NP_001350654.1:p.Asn784His
NM_001371656.1:c.4729A>C	NP_001358585.1:p.Asn1577His
NM_001374820.1:c.4729A>C	NP_001361749.1:p.Asn1577His
NM_001374828.1:c.4849A>C MANE Select	NP_001361757.1:p.Asn1617His
NM_017519.3:c.4690A>C	NP_059989.3:p.Asn1564His