Canonical Allele Identifier: CA366230318

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128325214
• MyVariant Identifiers: chr6:g.157505444A>T (hg19) ; chr6:g.157184310A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157184310A>T , CM000668.2:g.157184310A>T	GRCh38
NC_000006.11:g.157505444A>T , CM000668.1:g.157505444A>T	GRCh37
NC_000006.10:g.157547136A>T	NCBI36
NG_032093.1:g.411381A>T
NG_032093.2:g.411381A>T
NG_066624.1:g.413285A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.3635A>T	ENSP00000055163.8:p.Lys1212Ile
ENST00000414678.8:c.3704A>T	ENSP00000412835.3:p.Lys1235Ile
ENST00000637015.2:c.3923A>T	ENSP00000489729.2:p.Lys1308Ile
ENST00000319584.11:c.1808A>T	ENSP00000313006.7:p.Lys603Ile
ENST00000346085.10:c.3674A>T	ENSP00000344546.5:p.Lys1225Ile
ENST00000350026.10:c.3386A>T	ENSP00000055163.7:p.Lys1129Ile
ENST00000414678.7:c.1952A>T	ENSP00000412835.2:p.Lys651Ile
ENST00000635849.1:c.1115A>T	ENSP00000490948.1:p.Lys372Ile
ENST00000635957.1:c.749A>T	ENSP00000490385.1:p.Lys250Ile
ENST00000636930.2:c.3794A>T MANE Select	ENSP00000490491.2:p.Lys1265Ile
ENST00000636940.1:n.1791A>T
ENST00000637015.1:c.1162A>T
ENST00000637568.1:c.1076A>T
ENST00000637741.1:n.460A>T
ENST00000637810.1:c.1136A>T	ENSP00000489636.1:p.Lys379Ile
ENST00000637904.1:c.1295A>T	ENSP00000490550.1:p.Lys432Ile
ENST00000647938.1:c.3425A>T	ENSP00000498155.1:p.Lys1142Ile
ENST00000319584.10:c.1811A>T	ENSP00000313006.6:p.Lys604Ile
ENST00000346085.9:c.3425A>T	ENSP00000344546.4:p.Lys1142Ile
ENST00000350026.9:c.3386A>T	ENSP00000055163.7:p.Lys1129Ile
ENST00000400790.3:c.587A>T	ENSP00000383596.3:p.Lys196Ile
ENST00000414678.6:c.1952A>T	ENSP00000412835.2:p.Lys651Ile
NM_017519.2:c.3386A>T	NP_059989.2:p.Lys1129Ile
NM_020732.3:c.3425A>T	NP_065783.3:p.Lys1142Ile
XM_005267069.3:c.3545A>T	XP_005267126.2:p.Lys1182Ile
XM_011535984.1:c.2624A>T	XP_011534286.1:p.Lys875Ile
XM_011535985.1:c.2444A>T	XP_011534287.1:p.Lys815Ile
XM_011535986.1:c.2204A>T	XP_011534288.1:p.Lys735Ile
XM_011535987.1:c.1823A>T	XP_011534289.1:p.Lys608Ile
XM_011535988.1:c.686A>T	XP_011534290.1:p.Lys229Ile
NM_001346813.1:c.3545A>T	NP_001333742.1:p.Lys1182Ile
NM_001363725.1:c.1295A>T	NP_001350654.1:p.Lys432Ile
XM_011535984.2:c.3755A>T	XP_011534286.2:p.Lys1252Ile
XM_011535988.3:c.686A>T	XP_011534290.1:p.Lys229Ile
XM_017011103.2:c.3656A>T	XP_016866592.1:p.Lys1219Ile
XM_017011104.1:c.3626A>T	XP_016866593.1:p.Lys1209Ile
XM_017011105.2:c.3596A>T	XP_016866594.1:p.Lys1199Ile
XM_017011106.2:c.3467A>T	XP_016866595.1:p.Lys1156Ile
XM_017011107.2:c.3446A>T	XP_016866596.1:p.Lys1149Ile
XR_002956289.1:n.3838A>T
NM_001363725.2:c.1295A>T	NP_001350654.1:p.Lys432Ile
NM_001371656.1:c.3674A>T	NP_001358585.1:p.Lys1225Ile
NM_001374820.1:c.3674A>T	NP_001361749.1:p.Lys1225Ile
NM_001374828.1:c.3794A>T MANE Select	NP_001361757.1:p.Lys1265Ile
NM_017519.3:c.3635A>T	NP_059989.3:p.Lys1212Ile