Canonical Allele Identifier: CA821328185

Gene: ARID1B

Linked Data

• dbSNP Id: rs1159801974
• MyVariant Identifiers: chr6:g.157469589_157469590del (hg19) ; chr6:g.157148455_157148456del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148461_157148462del , CM000668.2:g.157148461_157148462del	GRCh38
NC_000006.11:g.157469595_157469596del , CM000668.1:g.157469595_157469596del	GRCh37
NC_000006.10:g.157511287_157511288del	NCBI36
NG_032093.1:g.375532_375533del
NG_032093.2:g.375532_375533del
NG_066624.1:g.377436_377437del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2762-163_2762-162del	ENSP00000055163.8:n.2762-163_2762-162del
ENST00000414678.8:c.2672-163_2672-162del	ENSP00000412835.3:n.2672-163_2672-162del
ENST00000637015.2:c.2762-163_2762-162del	ENSP00000489729.2:n.2762-163_2762-162del
ENST00000319584.11:c.776-163_776-162del	ENSP00000313006.7:n.776-163_776-162del
ENST00000346085.10:c.2801-163_2801-162del	ENSP00000344546.5:n.2801-163_2801-162del
ENST00000350026.10:c.2513-163_2513-162del	ENSP00000055163.7:n.2513-163_2513-162del
ENST00000414678.7:c.920-163_920-162del	ENSP00000412835.2:n.920-163_920-162del
ENST00000452544.2:n.663-163_663-162del
ENST00000635849.1:c.83-163_83-162del	ENSP00000490948.1:n.83-163_83-162del
ENST00000636930.2:c.2762-163_2762-162del MANE Select	ENSP00000490491.2:n.2762-163_2762-162del
ENST00000637810.1:c.263-163_263-162del	ENSP00000489636.1:n.263-163_263-162del
ENST00000637904.1:c.263-163_263-162del	ENSP00000490550.1:n.263-163_263-162del
ENST00000647938.1:c.2552-163_2552-162del	ENSP00000498155.1:n.2552-163_2552-162del
ENST00000674190.1:n.1511-163_1511-162del
ENST00000319584.10:c.779-163_779-162del	ENSP00000313006.6:n.779-163_779-162del
ENST00000346085.9:c.2552-163_2552-162del	ENSP00000344546.4:n.2552-163_2552-162del
ENST00000350026.9:c.2513-163_2513-162del	ENSP00000055163.7:n.2513-163_2513-162del
ENST00000414678.6:c.920-163_920-162del	ENSP00000412835.2:n.920-163_920-162del
ENST00000452544.1:n.609-163_609-162del
NM_017519.2:c.2513-163_2513-162del	NP_059989.2:n.2513-163_2513-162del
NM_020732.3:c.2552-163_2552-162del	NP_065783.3:n.2552-163_2552-162del
XM_005267069.3:c.2513-163_2513-162del	XP_005267126.2:n.2513-163_2513-162del
XM_011535984.1:c.1463-163_1463-162del	XP_011534286.1:n.1463-163_1463-162del
XM_011535985.1:c.1283-163_1283-162del	XP_011534287.1:n.1283-163_1283-162del
XM_011535986.1:c.1043-163_1043-162del	XP_011534288.1:n.1043-163_1043-162del
XM_011535987.1:c.662-163_662-162del	XP_011534289.1:n.662-163_662-162del
XM_011535988.1:c.-20+15254_-20+15255del	XP_011534290.1:n.-20+15254_-20+15255del
NM_001346813.1:c.2513-163_2513-162del	NP_001333742.1:n.2513-163_2513-162del
NM_001363725.1:c.263-163_263-162del	NP_001350654.1:n.263-163_263-162del
XM_011535984.2:c.2594-163_2594-162del	XP_011534286.2:n.2594-163_2594-162del
XM_011535988.3:c.-20+15254_-20+15255del	XP_011534290.1:n.-20+15254_-20+15255del
XM_017011103.2:c.2594-163_2594-162del	XP_016866592.1:n.2594-163_2594-162del
XM_017011104.1:c.2594-163_2594-162del	XP_016866593.1:n.2594-163_2594-162del
XM_017011105.2:c.2594-163_2594-162del	XP_016866594.1:n.2594-163_2594-162del
XM_017011106.2:c.2594-163_2594-162del	XP_016866595.1:n.2594-163_2594-162del
XM_017011107.2:c.2414-163_2414-162del	XP_016866596.1:n.2414-163_2414-162del
XR_002956289.1:n.2677-163_2677-162del
NM_001363725.2:c.263-163_263-162del	NP_001350654.1:n.263-163_263-162del
NM_001371656.1:c.2801-163_2801-162del	NP_001358585.1:n.2801-163_2801-162del
NM_001374820.1:c.2801-163_2801-162del	NP_001361749.1:n.2801-163_2801-162del
NM_001374828.1:c.2762-163_2762-162del MANE Select	NP_001361757.1:n.2762-163_2762-162del
NM_017519.3:c.2762-163_2762-162del	NP_059989.3:n.2762-163_2762-162del