Canonical Allele Identifier: CA366389255

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470058A>T (hg19) ; chr6:g.157148924A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148924A>T , CM000668.2:g.157148924A>T	GRCh38
NC_000006.11:g.157470058A>T , CM000668.1:g.157470058A>T	GRCh37
NC_000006.10:g.157511750A>T	NCBI36
NG_032093.1:g.375995A>T
NG_032093.2:g.375995A>T
NG_066624.1:g.377899A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3062A>T	ENSP00000055163.8:p.Gln1021Leu
ENST00000414678.8:c.2972A>T	ENSP00000412835.3:p.Gln991Leu
ENST00000637015.2:c.3062A>T	ENSP00000489729.2:p.Gln1021Leu
ENST00000319584.11:c.1076A>T	ENSP00000313006.7:p.Gln359Leu
ENST00000346085.10:c.3101A>T	ENSP00000344546.5:p.Gln1034Leu
ENST00000350026.10:c.2813A>T	ENSP00000055163.7:p.Gln938Leu
ENST00000414678.7:c.1220A>T	ENSP00000412835.2:p.Gln407Leu
ENST00000452544.2:n.963A>T
ENST00000635849.1:c.383A>T	ENSP00000490948.1:p.Gln128Leu
ENST00000635957.1:c.17A>T	ENSP00000490385.1:p.Gln6Leu
ENST00000636426.1:n.196A>T
ENST00000636930.2:c.3062A>T MANE Select	ENSP00000490491.2:p.Gln1021Leu
ENST00000637015.1:c.301A>T
ENST00000637568.1:c.105A>T
ENST00000637810.1:c.563A>T	ENSP00000489636.1:p.Gln188Leu
ENST00000637904.1:c.563A>T	ENSP00000490550.1:p.Gln188Leu
ENST00000647938.1:c.2852A>T	ENSP00000498155.1:p.Gln951Leu
ENST00000674190.1:n.1811A>T
ENST00000319584.10:c.1079A>T	ENSP00000313006.6:p.Gln360Leu
ENST00000346085.9:c.2852A>T	ENSP00000344546.4:p.Gln951Leu
ENST00000350026.9:c.2813A>T	ENSP00000055163.7:p.Gln938Leu
ENST00000400790.3:c.14A>T	ENSP00000383596.3:p.Gln5Leu
ENST00000414678.6:c.1220A>T	ENSP00000412835.2:p.Gln407Leu
ENST00000452544.1:n.909A>T
ENST00000478761.3:c.135A>T
NM_017519.2:c.2813A>T	NP_059989.2:p.Gln938Leu
NM_020732.3:c.2852A>T	NP_065783.3:p.Gln951Leu
XM_005267069.3:c.2813A>T	XP_005267126.2:p.Gln938Leu
XM_011535984.1:c.1763A>T	XP_011534286.1:p.Gln588Leu
XM_011535985.1:c.1583A>T	XP_011534287.1:p.Gln528Leu
XM_011535986.1:c.1343A>T	XP_011534288.1:p.Gln448Leu
XM_011535987.1:c.962A>T	XP_011534289.1:p.Gln321Leu
XM_011535988.1:c.-20+15717A>T	XP_011534290.1:n.-20+15717A>T
NM_001346813.1:c.2813A>T	NP_001333742.1:p.Gln938Leu
NM_001363725.1:c.563A>T	NP_001350654.1:p.Gln188Leu
XM_011535984.2:c.2894A>T	XP_011534286.2:p.Gln965Leu
XM_011535988.3:c.-20+15717A>T	XP_011534290.1:n.-20+15717A>T
XM_017011103.2:c.2894A>T	XP_016866592.1:p.Gln965Leu
XM_017011104.1:c.2894A>T	XP_016866593.1:p.Gln965Leu
XM_017011105.2:c.2894A>T	XP_016866594.1:p.Gln965Leu
XM_017011106.2:c.2894A>T	XP_016866595.1:p.Gln965Leu
XM_017011107.2:c.2714A>T	XP_016866596.1:p.Gln905Leu
XR_002956289.1:n.2977A>T
NM_001363725.2:c.563A>T	NP_001350654.1:p.Gln188Leu
NM_001371656.1:c.3101A>T	NP_001358585.1:p.Gln1034Leu
NM_001374820.1:c.3101A>T	NP_001361749.1:p.Gln1034Leu
NM_001374828.1:c.3062A>T MANE Select	NP_001361757.1:p.Gln1021Leu
NM_017519.3:c.3062A>T	NP_059989.3:p.Gln1021Leu