Canonical Allele Identifier: CA366234026

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510792G>C (hg19) ; chr6:g.157189658G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189658G>C , CM000668.2:g.157189658G>C	GRCh38
NC_000006.11:g.157510792G>C , CM000668.1:g.157510792G>C	GRCh37
NC_000006.10:g.157552484G>C	NCBI36
NG_032093.1:g.416729G>C
NG_032093.2:g.416729G>C
NG_066624.1:g.418633G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3777G>C	ENSP00000055163.8:p.Leu1259Phe
ENST00000414678.8:c.3846G>C	ENSP00000412835.3:p.Leu1282Phe
ENST00000637015.2:c.4065G>C	ENSP00000489729.2:p.Leu1355Phe
ENST00000346085.10:c.3816G>C	ENSP00000344546.5:p.Leu1272Phe
ENST00000350026.10:c.3528G>C	ENSP00000055163.7:p.Leu1176Phe
ENST00000414678.7:c.2094G>C	ENSP00000412835.2:p.Leu698Phe
ENST00000635849.1:c.1257G>C	ENSP00000490948.1:p.Leu419Phe
ENST00000635957.1:c.891G>C	ENSP00000490385.1:p.Leu297Phe
ENST00000636930.2:c.3936G>C MANE Select	ENSP00000490491.2:p.Leu1312Phe
ENST00000636940.1:n.1933G>C
ENST00000637015.1:c.1304G>C
ENST00000637568.1:c.1218G>C
ENST00000637741.1:n.602G>C
ENST00000637810.1:c.1278G>C	ENSP00000489636.1:p.Leu426Phe
ENST00000637904.1:c.1437G>C	ENSP00000490550.1:p.Leu479Phe
ENST00000647938.1:c.3567G>C	ENSP00000498155.1:p.Leu1189Phe
ENST00000346085.9:c.3567G>C	ENSP00000344546.4:p.Leu1189Phe
ENST00000350026.9:c.3528G>C	ENSP00000055163.7:p.Leu1176Phe
ENST00000414678.6:c.2094G>C	ENSP00000412835.2:p.Leu698Phe
NM_017519.2:c.3528G>C	NP_059989.2:p.Leu1176Phe
NM_020732.3:c.3567G>C	NP_065783.3:p.Leu1189Phe
XM_005267069.3:c.3687G>C	XP_005267126.2:p.Leu1229Phe
XM_011535984.1:c.2766G>C	XP_011534286.1:p.Leu922Phe
XM_011535985.1:c.2586G>C	XP_011534287.1:p.Leu862Phe
XM_011535986.1:c.2346G>C	XP_011534288.1:p.Leu782Phe
XM_011535987.1:c.1965G>C	XP_011534289.1:p.Leu655Phe
XM_011535988.1:c.828G>C	XP_011534290.1:p.Leu276Phe
NM_001346813.1:c.3687G>C	NP_001333742.1:p.Leu1229Phe
NM_001363725.1:c.1437G>C	NP_001350654.1:p.Leu479Phe
XM_011535984.2:c.3897G>C	XP_011534286.2:p.Leu1299Phe
XM_011535988.3:c.828G>C	XP_011534290.1:p.Leu276Phe
XM_017011103.2:c.3798G>C	XP_016866592.1:p.Leu1266Phe
XM_017011104.1:c.3768G>C	XP_016866593.1:p.Leu1256Phe
XM_017011105.2:c.3738G>C	XP_016866594.1:p.Leu1246Phe
XM_017011106.2:c.3609G>C	XP_016866595.1:p.Leu1203Phe
XM_017011107.2:c.3588G>C	XP_016866596.1:p.Leu1196Phe
XR_002956289.1:n.3980G>C
NM_001363725.2:c.1437G>C	NP_001350654.1:p.Leu479Phe
NM_001371656.1:c.3816G>C	NP_001358585.1:p.Leu1272Phe
NM_001374820.1:c.3816G>C	NP_001361749.1:p.Leu1272Phe
NM_001374828.1:c.3936G>C MANE Select	NP_001361757.1:p.Leu1312Phe
NM_017519.3:c.3777G>C	NP_059989.3:p.Leu1259Phe