Canonical Allele Identifier: CA150846236

Gene: ARID1B

Linked Data

• dbSNP Id: rs992264559
• gnomAD v3: 6-157148511-AC-A
• gnomAD v4: 6-157148511-AC-A
• MyVariant Identifiers: chr6:g.157469646del (hg19) ; chr6:g.157148512del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148512del , CM000668.2:g.157148512del	GRCh38
NC_000006.11:g.157469646del , CM000668.1:g.157469646del	GRCh37
NC_000006.10:g.157511338del	NCBI36
NG_032093.1:g.375583del
NG_032093.2:g.375583del
NG_066624.1:g.377487del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2762-112del	ENSP00000055163.8:n.2762-112del
ENST00000414678.8:c.2672-112del	ENSP00000412835.3:n.2672-112del
ENST00000637015.2:c.2762-112del	ENSP00000489729.2:n.2762-112del
ENST00000319584.11:c.776-112del	ENSP00000313006.7:n.776-112del
ENST00000346085.10:c.2801-112del	ENSP00000344546.5:n.2801-112del
ENST00000350026.10:c.2513-112del	ENSP00000055163.7:n.2513-112del
ENST00000414678.7:c.920-112del	ENSP00000412835.2:n.920-112del
ENST00000452544.2:n.663-112del
ENST00000635849.1:c.83-112del	ENSP00000490948.1:n.83-112del
ENST00000636930.2:c.2762-112del MANE Select	ENSP00000490491.2:n.2762-112del
ENST00000637810.1:c.263-112del	ENSP00000489636.1:n.263-112del
ENST00000637904.1:c.263-112del	ENSP00000490550.1:n.263-112del
ENST00000647938.1:c.2552-112del	ENSP00000498155.1:n.2552-112del
ENST00000674190.1:n.1511-112del
ENST00000319584.10:c.779-112del	ENSP00000313006.6:n.779-112del
ENST00000346085.9:c.2552-112del	ENSP00000344546.4:n.2552-112del
ENST00000350026.9:c.2513-112del	ENSP00000055163.7:n.2513-112del
ENST00000414678.6:c.920-112del	ENSP00000412835.2:n.920-112del
ENST00000452544.1:n.609-112del
NM_017519.2:c.2513-112del	NP_059989.2:n.2513-112del
NM_020732.3:c.2552-112del	NP_065783.3:n.2552-112del
XM_005267069.3:c.2513-112del	XP_005267126.2:n.2513-112del
XM_011535984.1:c.1463-112del	XP_011534286.1:n.1463-112del
XM_011535985.1:c.1283-112del	XP_011534287.1:n.1283-112del
XM_011535986.1:c.1043-112del	XP_011534288.1:n.1043-112del
XM_011535987.1:c.662-112del	XP_011534289.1:n.662-112del
XM_011535988.1:c.-20+15305del	XP_011534290.1:n.-20+15305del
NM_001346813.1:c.2513-112del	NP_001333742.1:n.2513-112del
NM_001363725.1:c.263-112del	NP_001350654.1:n.263-112del
XM_011535984.2:c.2594-112del	XP_011534286.2:n.2594-112del
XM_011535988.3:c.-20+15305del	XP_011534290.1:n.-20+15305del
XM_017011103.2:c.2594-112del	XP_016866592.1:n.2594-112del
XM_017011104.1:c.2594-112del	XP_016866593.1:n.2594-112del
XM_017011105.2:c.2594-112del	XP_016866594.1:n.2594-112del
XM_017011106.2:c.2594-112del	XP_016866595.1:n.2594-112del
XM_017011107.2:c.2414-112del	XP_016866596.1:n.2414-112del
XR_002956289.1:n.2677-112del
NM_001363725.2:c.263-112del	NP_001350654.1:n.263-112del
NM_001371656.1:c.2801-112del	NP_001358585.1:n.2801-112del
NM_001374820.1:c.2801-112del	NP_001361749.1:n.2801-112del
NM_001374828.1:c.2762-112del MANE Select	NP_001361757.1:n.2762-112del
NM_017519.3:c.2762-112del	NP_059989.3:n.2762-112del