Canonical Allele Identifier: CA366234023

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157510791T>C (hg19) ; chr6:g.157189657T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189657T>C , CM000668.2:g.157189657T>C	GRCh38
NC_000006.11:g.157510791T>C , CM000668.1:g.157510791T>C	GRCh37
NC_000006.10:g.157552483T>C	NCBI36
NG_032093.1:g.416728T>C
NG_032093.2:g.416728T>C
NG_066624.1:g.418632T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3776T>C	ENSP00000055163.8:p.Leu1259Ser
ENST00000414678.8:c.3845T>C	ENSP00000412835.3:p.Leu1282Ser
ENST00000637015.2:c.4064T>C	ENSP00000489729.2:p.Leu1355Ser
ENST00000346085.10:c.3815T>C	ENSP00000344546.5:p.Leu1272Ser
ENST00000350026.10:c.3527T>C	ENSP00000055163.7:p.Leu1176Ser
ENST00000414678.7:c.2093T>C	ENSP00000412835.2:p.Leu698Ser
ENST00000635849.1:c.1256T>C	ENSP00000490948.1:p.Leu419Ser
ENST00000635957.1:c.890T>C	ENSP00000490385.1:p.Leu297Ser
ENST00000636930.2:c.3935T>C MANE Select	ENSP00000490491.2:p.Leu1312Ser
ENST00000636940.1:n.1932T>C
ENST00000637015.1:c.1303T>C
ENST00000637568.1:c.1217T>C
ENST00000637741.1:n.601T>C
ENST00000637810.1:c.1277T>C	ENSP00000489636.1:p.Leu426Ser
ENST00000637904.1:c.1436T>C	ENSP00000490550.1:p.Leu479Ser
ENST00000647938.1:c.3566T>C	ENSP00000498155.1:p.Leu1189Ser
ENST00000346085.9:c.3566T>C	ENSP00000344546.4:p.Leu1189Ser
ENST00000350026.9:c.3527T>C	ENSP00000055163.7:p.Leu1176Ser
ENST00000414678.6:c.2093T>C	ENSP00000412835.2:p.Leu698Ser
NM_017519.2:c.3527T>C	NP_059989.2:p.Leu1176Ser
NM_020732.3:c.3566T>C	NP_065783.3:p.Leu1189Ser
XM_005267069.3:c.3686T>C	XP_005267126.2:p.Leu1229Ser
XM_011535984.1:c.2765T>C	XP_011534286.1:p.Leu922Ser
XM_011535985.1:c.2585T>C	XP_011534287.1:p.Leu862Ser
XM_011535986.1:c.2345T>C	XP_011534288.1:p.Leu782Ser
XM_011535987.1:c.1964T>C	XP_011534289.1:p.Leu655Ser
XM_011535988.1:c.827T>C	XP_011534290.1:p.Leu276Ser
NM_001346813.1:c.3686T>C	NP_001333742.1:p.Leu1229Ser
NM_001363725.1:c.1436T>C	NP_001350654.1:p.Leu479Ser
XM_011535984.2:c.3896T>C	XP_011534286.2:p.Leu1299Ser
XM_011535988.3:c.827T>C	XP_011534290.1:p.Leu276Ser
XM_017011103.2:c.3797T>C	XP_016866592.1:p.Leu1266Ser
XM_017011104.1:c.3767T>C	XP_016866593.1:p.Leu1256Ser
XM_017011105.2:c.3737T>C	XP_016866594.1:p.Leu1246Ser
XM_017011106.2:c.3608T>C	XP_016866595.1:p.Leu1203Ser
XM_017011107.2:c.3587T>C	XP_016866596.1:p.Leu1196Ser
XR_002956289.1:n.3979T>C
NM_001363725.2:c.1436T>C	NP_001350654.1:p.Leu479Ser
NM_001371656.1:c.3815T>C	NP_001358585.1:p.Leu1272Ser
NM_001374820.1:c.3815T>C	NP_001361749.1:p.Leu1272Ser
NM_001374828.1:c.3935T>C MANE Select	NP_001361757.1:p.Leu1312Ser
NM_017519.3:c.3776T>C	NP_059989.3:p.Leu1259Ser