Canonical Allele Identifier: CA366389230

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128634969
• gnomAD v4: 6-157148914-G-A
• MyVariant Identifiers: chr6:g.157470048G>A (hg19) ; chr6:g.157148914G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148914G>A , CM000668.2:g.157148914G>A	GRCh38
NC_000006.11:g.157470048G>A , CM000668.1:g.157470048G>A	GRCh37
NC_000006.10:g.157511740G>A	NCBI36
NG_032093.1:g.375985G>A
NG_032093.2:g.375985G>A
NG_066624.1:g.377889G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3052G>A	ENSP00000055163.8:p.Ala1018Thr
ENST00000414678.8:c.2962G>A	ENSP00000412835.3:p.Ala988Thr
ENST00000637015.2:c.3052G>A	ENSP00000489729.2:p.Ala1018Thr
ENST00000319584.11:c.1066G>A	ENSP00000313006.7:p.Ala356Thr
ENST00000346085.10:c.3091G>A	ENSP00000344546.5:p.Ala1031Thr
ENST00000350026.10:c.2803G>A	ENSP00000055163.7:p.Ala935Thr
ENST00000414678.7:c.1210G>A	ENSP00000412835.2:p.Ala404Thr
ENST00000452544.2:n.953G>A
ENST00000635849.1:c.373G>A	ENSP00000490948.1:p.Ala125Thr
ENST00000635957.1:c.7G>A	ENSP00000490385.1:p.Ala3Thr
ENST00000636426.1:n.186G>A
ENST00000636930.2:c.3052G>A MANE Select	ENSP00000490491.2:p.Ala1018Thr
ENST00000637015.1:c.291G>A
ENST00000637568.1:c.95G>A
ENST00000637810.1:c.553G>A	ENSP00000489636.1:p.Ala185Thr
ENST00000637904.1:c.553G>A	ENSP00000490550.1:p.Ala185Thr
ENST00000647938.1:c.2842G>A	ENSP00000498155.1:p.Ala948Thr
ENST00000674190.1:n.1801G>A
ENST00000319584.10:c.1069G>A	ENSP00000313006.6:p.Ala357Thr
ENST00000346085.9:c.2842G>A	ENSP00000344546.4:p.Ala948Thr
ENST00000350026.9:c.2803G>A	ENSP00000055163.7:p.Ala935Thr
ENST00000400790.3:c.4G>A	ENSP00000383596.3:p.Ala2Thr
ENST00000414678.6:c.1210G>A	ENSP00000412835.2:p.Ala404Thr
ENST00000452544.1:n.899G>A
ENST00000478761.3:c.125G>A
NM_017519.2:c.2803G>A	NP_059989.2:p.Ala935Thr
NM_020732.3:c.2842G>A	NP_065783.3:p.Ala948Thr
XM_005267069.3:c.2803G>A	XP_005267126.2:p.Ala935Thr
XM_011535984.1:c.1753G>A	XP_011534286.1:p.Ala585Thr
XM_011535985.1:c.1573G>A	XP_011534287.1:p.Ala525Thr
XM_011535986.1:c.1333G>A	XP_011534288.1:p.Ala445Thr
XM_011535987.1:c.952G>A	XP_011534289.1:p.Ala318Thr
XM_011535988.1:c.-20+15707G>A	XP_011534290.1:n.-20+15707G>A
NM_001346813.1:c.2803G>A	NP_001333742.1:p.Ala935Thr
NM_001363725.1:c.553G>A	NP_001350654.1:p.Ala185Thr
XM_011535984.2:c.2884G>A	XP_011534286.2:p.Ala962Thr
XM_011535988.3:c.-20+15707G>A	XP_011534290.1:n.-20+15707G>A
XM_017011103.2:c.2884G>A	XP_016866592.1:p.Ala962Thr
XM_017011104.1:c.2884G>A	XP_016866593.1:p.Ala962Thr
XM_017011105.2:c.2884G>A	XP_016866594.1:p.Ala962Thr
XM_017011106.2:c.2884G>A	XP_016866595.1:p.Ala962Thr
XM_017011107.2:c.2704G>A	XP_016866596.1:p.Ala902Thr
XR_002956289.1:n.2967G>A
NM_001363725.2:c.553G>A	NP_001350654.1:p.Ala185Thr
NM_001371656.1:c.3091G>A	NP_001358585.1:p.Ala1031Thr
NM_001374820.1:c.3091G>A	NP_001361749.1:p.Ala1031Thr
NM_001374828.1:c.3052G>A MANE Select	NP_001361757.1:p.Ala1018Thr
NM_017519.3:c.3052G>A	NP_059989.3:p.Ala1018Thr