Canonical Allele Identifier: CA366388673

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128633983
• MyVariant Identifiers: chr6:g.157469791T>G (hg19) ; chr6:g.157148657T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148657T>G , CM000668.2:g.157148657T>G	GRCh38
NC_000006.11:g.157469791T>G , CM000668.1:g.157469791T>G	GRCh37
NC_000006.10:g.157511483T>G	NCBI36
NG_032093.1:g.375728T>G
NG_032093.2:g.375728T>G
NG_066624.1:g.377632T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2795T>G	ENSP00000055163.8:p.Val932Gly
ENST00000414678.8:c.2705T>G	ENSP00000412835.3:p.Val902Gly
ENST00000637015.2:c.2795T>G	ENSP00000489729.2:p.Val932Gly
ENST00000319584.11:c.809T>G	ENSP00000313006.7:p.Val270Gly
ENST00000346085.10:c.2834T>G	ENSP00000344546.5:p.Val945Gly
ENST00000350026.10:c.2546T>G	ENSP00000055163.7:p.Val849Gly
ENST00000414678.7:c.953T>G	ENSP00000412835.2:p.Val318Gly
ENST00000452544.2:n.696T>G
ENST00000635849.1:c.116T>G	ENSP00000490948.1:p.Val39Gly
ENST00000636930.2:c.2795T>G MANE Select	ENSP00000490491.2:p.Val932Gly
ENST00000637015.1:c.34T>G
ENST00000637810.1:c.296T>G	ENSP00000489636.1:p.Val99Gly
ENST00000637904.1:c.296T>G	ENSP00000490550.1:p.Val99Gly
ENST00000647938.1:c.2585T>G	ENSP00000498155.1:p.Val862Gly
ENST00000674190.1:n.1544T>G
ENST00000319584.10:c.812T>G	ENSP00000313006.6:p.Val271Gly
ENST00000346085.9:c.2585T>G	ENSP00000344546.4:p.Val862Gly
ENST00000350026.9:c.2546T>G	ENSP00000055163.7:p.Val849Gly
ENST00000414678.6:c.953T>G	ENSP00000412835.2:p.Val318Gly
ENST00000452544.1:n.642T>G
NM_017519.2:c.2546T>G	NP_059989.2:p.Val849Gly
NM_020732.3:c.2585T>G	NP_065783.3:p.Val862Gly
XM_005267069.3:c.2546T>G	XP_005267126.2:p.Val849Gly
XM_011535984.1:c.1496T>G	XP_011534286.1:p.Val499Gly
XM_011535985.1:c.1316T>G	XP_011534287.1:p.Val439Gly
XM_011535986.1:c.1076T>G	XP_011534288.1:p.Val359Gly
XM_011535987.1:c.695T>G	XP_011534289.1:p.Val232Gly
XM_011535988.1:c.-20+15450T>G	XP_011534290.1:n.-20+15450T>G
NM_001346813.1:c.2546T>G	NP_001333742.1:p.Val849Gly
NM_001363725.1:c.296T>G	NP_001350654.1:p.Val99Gly
XM_011535984.2:c.2627T>G	XP_011534286.2:p.Val876Gly
XM_011535988.3:c.-20+15450T>G	XP_011534290.1:n.-20+15450T>G
XM_017011103.2:c.2627T>G	XP_016866592.1:p.Val876Gly
XM_017011104.1:c.2627T>G	XP_016866593.1:p.Val876Gly
XM_017011105.2:c.2627T>G	XP_016866594.1:p.Val876Gly
XM_017011106.2:c.2627T>G	XP_016866595.1:p.Val876Gly
XM_017011107.2:c.2447T>G	XP_016866596.1:p.Val816Gly
XR_002956289.1:n.2710T>G
NM_001363725.2:c.296T>G	NP_001350654.1:p.Val99Gly
NM_001371656.1:c.2834T>G	NP_001358585.1:p.Val945Gly
NM_001374820.1:c.2834T>G	NP_001361749.1:p.Val945Gly
NM_001374828.1:c.2795T>G MANE Select	NP_001361757.1:p.Val932Gly
NM_017519.3:c.2795T>G	NP_059989.3:p.Val932Gly