Canonical Allele Identifier: CA366242028

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522248A>C (hg19) ; chr6:g.157201114A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201114A>C , CM000668.2:g.157201114A>C	GRCh38
NC_000006.11:g.157522248A>C , CM000668.1:g.157522248A>C	GRCh37
NC_000006.10:g.157563940A>C	NCBI36
NG_032093.1:g.428185A>C
NG_032093.2:g.428185A>C
NG_066624.1:g.430089A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4730A>C	ENSP00000055163.8:p.Asn1577Thr
ENST00000414678.8:c.4799A>C	ENSP00000412835.3:p.Asn1600Thr
ENST00000637015.2:c.5018A>C	ENSP00000489729.2:p.Asn1673Thr
ENST00000346085.10:c.4769A>C	ENSP00000344546.5:p.Asn1590Thr
ENST00000350026.10:c.4481A>C	ENSP00000055163.7:p.Asn1494Thr
ENST00000414678.7:c.3047A>C	ENSP00000412835.2:p.Asn1016Thr
ENST00000635849.1:c.2210A>C	ENSP00000490948.1:p.Asn737Thr
ENST00000635957.1:c.1841A>C	ENSP00000490385.1:p.Asn614Thr
ENST00000636227.1:n.3352A>C
ENST00000636254.1:n.809A>C
ENST00000636930.2:c.4889A>C MANE Select	ENSP00000490491.2:p.Asn1630Thr
ENST00000636940.1:n.2886A>C
ENST00000637015.1:c.2257A>C
ENST00000637568.1:c.2171A>C
ENST00000637741.1:n.1555A>C
ENST00000637810.1:c.2231A>C	ENSP00000489636.1:p.Asn744Thr
ENST00000637904.1:c.2390A>C	ENSP00000490550.1:p.Asn797Thr
ENST00000647938.1:c.4520A>C	ENSP00000498155.1:p.Asn1507Thr
ENST00000346085.9:c.4520A>C	ENSP00000344546.4:p.Asn1507Thr
ENST00000350026.9:c.4481A>C	ENSP00000055163.7:p.Asn1494Thr
ENST00000414678.6:c.3047A>C	ENSP00000412835.2:p.Asn1016Thr
NM_017519.2:c.4481A>C	NP_059989.2:p.Asn1494Thr
NM_020732.3:c.4520A>C	NP_065783.3:p.Asn1507Thr
XM_005267069.3:c.4640A>C	XP_005267126.2:p.Asn1547Thr
XM_011535984.1:c.3719A>C	XP_011534286.1:p.Asn1240Thr
XM_011535985.1:c.3539A>C	XP_011534287.1:p.Asn1180Thr
XM_011535986.1:c.3299A>C	XP_011534288.1:p.Asn1100Thr
XM_011535987.1:c.2918A>C	XP_011534289.1:p.Asn973Thr
XM_011535988.1:c.1781A>C	XP_011534290.1:p.Asn594Thr
NM_001346813.1:c.4640A>C	NP_001333742.1:p.Asn1547Thr
NM_001363725.1:c.2390A>C	NP_001350654.1:p.Asn797Thr
XM_011535984.2:c.4850A>C	XP_011534286.2:p.Asn1617Thr
XM_011535988.3:c.1781A>C	XP_011534290.1:p.Asn594Thr
XM_017011103.2:c.4751A>C	XP_016866592.1:p.Asn1584Thr
XM_017011104.1:c.4721A>C	XP_016866593.1:p.Asn1574Thr
XM_017011105.2:c.4691A>C	XP_016866594.1:p.Asn1564Thr
XM_017011106.2:c.4562A>C	XP_016866595.1:p.Asn1521Thr
XM_017011107.2:c.4541A>C	XP_016866596.1:p.Asn1514Thr
XR_002956289.1:n.4836A>C
NM_001363725.2:c.2390A>C	NP_001350654.1:p.Asn797Thr
NM_001371656.1:c.4769A>C	NP_001358585.1:p.Asn1590Thr
NM_001374820.1:c.4769A>C	NP_001361749.1:p.Asn1590Thr
NM_001374828.1:c.4889A>C MANE Select	NP_001361757.1:p.Asn1630Thr
NM_017519.3:c.4730A>C	NP_059989.3:p.Asn1577Thr