Canonical Allele Identifier: CA366240892

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157521906A>C (hg19) ; chr6:g.157200772A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200772A>C , CM000668.2:g.157200772A>C	GRCh38
NC_000006.11:g.157521906A>C , CM000668.1:g.157521906A>C	GRCh37
NC_000006.10:g.157563598A>C	NCBI36
NG_032093.1:g.427843A>C
NG_032093.2:g.427843A>C
NG_066624.1:g.429747A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4388A>C	ENSP00000055163.8:p.Asn1463Thr
ENST00000414678.8:c.4457A>C	ENSP00000412835.3:p.Asn1486Thr
ENST00000637015.2:c.4676A>C	ENSP00000489729.2:p.Asn1559Thr
ENST00000346085.10:c.4427A>C	ENSP00000344546.5:p.Asn1476Thr
ENST00000350026.10:c.4139A>C	ENSP00000055163.7:p.Asn1380Thr
ENST00000414678.7:c.2705A>C	ENSP00000412835.2:p.Asn902Thr
ENST00000635849.1:c.1868A>C	ENSP00000490948.1:p.Asn623Thr
ENST00000635957.1:c.1499A>C	ENSP00000490385.1:p.Asn500Thr
ENST00000636227.1:n.3010A>C
ENST00000636254.1:n.467A>C
ENST00000636930.2:c.4547A>C MANE Select	ENSP00000490491.2:p.Asn1516Thr
ENST00000636940.1:n.2544A>C
ENST00000637015.1:c.1915A>C
ENST00000637568.1:c.1829A>C
ENST00000637741.1:n.1213A>C
ENST00000637810.1:c.1889A>C	ENSP00000489636.1:p.Asn630Thr
ENST00000637904.1:c.2048A>C	ENSP00000490550.1:p.Asn683Thr
ENST00000647938.1:c.4178A>C	ENSP00000498155.1:p.Asn1393Thr
ENST00000346085.9:c.4178A>C	ENSP00000344546.4:p.Asn1393Thr
ENST00000350026.9:c.4139A>C	ENSP00000055163.7:p.Asn1380Thr
ENST00000414678.6:c.2705A>C	ENSP00000412835.2:p.Asn902Thr
NM_017519.2:c.4139A>C	NP_059989.2:p.Asn1380Thr
NM_020732.3:c.4178A>C	NP_065783.3:p.Asn1393Thr
XM_005267069.3:c.4298A>C	XP_005267126.2:p.Asn1433Thr
XM_011535984.1:c.3377A>C	XP_011534286.1:p.Asn1126Thr
XM_011535985.1:c.3197A>C	XP_011534287.1:p.Asn1066Thr
XM_011535986.1:c.2957A>C	XP_011534288.1:p.Asn986Thr
XM_011535987.1:c.2576A>C	XP_011534289.1:p.Asn859Thr
XM_011535988.1:c.1439A>C	XP_011534290.1:p.Asn480Thr
NM_001346813.1:c.4298A>C	NP_001333742.1:p.Asn1433Thr
NM_001363725.1:c.2048A>C	NP_001350654.1:p.Asn683Thr
XM_011535984.2:c.4508A>C	XP_011534286.2:p.Asn1503Thr
XM_011535988.3:c.1439A>C	XP_011534290.1:p.Asn480Thr
XM_017011103.2:c.4409A>C	XP_016866592.1:p.Asn1470Thr
XM_017011104.1:c.4379A>C	XP_016866593.1:p.Asn1460Thr
XM_017011105.2:c.4349A>C	XP_016866594.1:p.Asn1450Thr
XM_017011106.2:c.4220A>C	XP_016866595.1:p.Asn1407Thr
XM_017011107.2:c.4199A>C	XP_016866596.1:p.Asn1400Thr
XR_002956289.1:n.4494A>C
NM_001363725.2:c.2048A>C	NP_001350654.1:p.Asn683Thr
NM_001371656.1:c.4427A>C	NP_001358585.1:p.Asn1476Thr
NM_001374820.1:c.4427A>C	NP_001361749.1:p.Asn1476Thr
NM_001374828.1:c.4547A>C MANE Select	NP_001361757.1:p.Asn1516Thr
NM_017519.3:c.4388A>C	NP_059989.3:p.Asn1463Thr