Canonical Allele Identifier: CA366240897

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157521908A>T (hg19) ; chr6:g.157200774A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157200774A>T , CM000668.2:g.157200774A>T	GRCh38
NC_000006.11:g.157521908A>T , CM000668.1:g.157521908A>T	GRCh37
NC_000006.10:g.157563600A>T	NCBI36
NG_032093.1:g.427845A>T
NG_032093.2:g.427845A>T
NG_066624.1:g.429749A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4390A>T	ENSP00000055163.8:p.Met1464Leu
ENST00000414678.8:c.4459A>T	ENSP00000412835.3:p.Met1487Leu
ENST00000637015.2:c.4678A>T	ENSP00000489729.2:p.Met1560Leu
ENST00000346085.10:c.4429A>T	ENSP00000344546.5:p.Met1477Leu
ENST00000350026.10:c.4141A>T	ENSP00000055163.7:p.Met1381Leu
ENST00000414678.7:c.2707A>T	ENSP00000412835.2:p.Met903Leu
ENST00000635849.1:c.1870A>T	ENSP00000490948.1:p.Met624Leu
ENST00000635957.1:c.1501A>T	ENSP00000490385.1:p.Met501Leu
ENST00000636227.1:n.3012A>T
ENST00000636254.1:n.469A>T
ENST00000636930.2:c.4549A>T MANE Select	ENSP00000490491.2:p.Met1517Leu
ENST00000636940.1:n.2546A>T
ENST00000637015.1:c.1917A>T
ENST00000637568.1:c.1831A>T
ENST00000637741.1:n.1215A>T
ENST00000637810.1:c.1891A>T	ENSP00000489636.1:p.Met631Leu
ENST00000637904.1:c.2050A>T	ENSP00000490550.1:p.Met684Leu
ENST00000647938.1:c.4180A>T	ENSP00000498155.1:p.Met1394Leu
ENST00000346085.9:c.4180A>T	ENSP00000344546.4:p.Met1394Leu
ENST00000350026.9:c.4141A>T	ENSP00000055163.7:p.Met1381Leu
ENST00000414678.6:c.2707A>T	ENSP00000412835.2:p.Met903Leu
NM_017519.2:c.4141A>T	NP_059989.2:p.Met1381Leu
NM_020732.3:c.4180A>T	NP_065783.3:p.Met1394Leu
XM_005267069.3:c.4300A>T	XP_005267126.2:p.Met1434Leu
XM_011535984.1:c.3379A>T	XP_011534286.1:p.Met1127Leu
XM_011535985.1:c.3199A>T	XP_011534287.1:p.Met1067Leu
XM_011535986.1:c.2959A>T	XP_011534288.1:p.Met987Leu
XM_011535987.1:c.2578A>T	XP_011534289.1:p.Met860Leu
XM_011535988.1:c.1441A>T	XP_011534290.1:p.Met481Leu
NM_001346813.1:c.4300A>T	NP_001333742.1:p.Met1434Leu
NM_001363725.1:c.2050A>T	NP_001350654.1:p.Met684Leu
XM_011535984.2:c.4510A>T	XP_011534286.2:p.Met1504Leu
XM_011535988.3:c.1441A>T	XP_011534290.1:p.Met481Leu
XM_017011103.2:c.4411A>T	XP_016866592.1:p.Met1471Leu
XM_017011104.1:c.4381A>T	XP_016866593.1:p.Met1461Leu
XM_017011105.2:c.4351A>T	XP_016866594.1:p.Met1451Leu
XM_017011106.2:c.4222A>T	XP_016866595.1:p.Met1408Leu
XM_017011107.2:c.4201A>T	XP_016866596.1:p.Met1401Leu
XR_002956289.1:n.4496A>T
NM_001363725.2:c.2050A>T	NP_001350654.1:p.Met684Leu
NM_001371656.1:c.4429A>T	NP_001358585.1:p.Met1477Leu
NM_001374820.1:c.4429A>T	NP_001361749.1:p.Met1477Leu
NM_001374828.1:c.4549A>T MANE Select	NP_001361757.1:p.Met1517Leu
NM_017519.3:c.4390A>T	NP_059989.3:p.Met1464Leu