Canonical Allele Identifier: CA2680917377

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157148510-A-AG

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148510_157148511insG , CM000668.2:g.157148510_157148511insG	GRCh38
NC_000006.11:g.157469644_157469645insG , CM000668.1:g.157469644_157469645insG	GRCh37
NC_000006.10:g.157511336_157511337insG	NCBI36
NG_032093.1:g.375581_375582insG
NG_032093.2:g.375581_375582insG
NG_066624.1:g.377485_377486insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2762-114_2762-113insG	ENSP00000055163.8:n.2762-114_2762-113insG
ENST00000414678.8:c.2672-114_2672-113insG	ENSP00000412835.3:n.2672-114_2672-113insG
ENST00000637015.2:c.2762-114_2762-113insG	ENSP00000489729.2:n.2762-114_2762-113insG
ENST00000319584.11:c.776-114_776-113insG	ENSP00000313006.7:n.776-114_776-113insG
ENST00000346085.10:c.2801-114_2801-113insG	ENSP00000344546.5:n.2801-114_2801-113insG
ENST00000350026.10:c.2513-114_2513-113insG	ENSP00000055163.7:n.2513-114_2513-113insG
ENST00000414678.7:c.920-114_920-113insG	ENSP00000412835.2:n.920-114_920-113insG
ENST00000452544.2:n.663-114_663-113insG
ENST00000635849.1:c.83-114_83-113insG	ENSP00000490948.1:n.83-114_83-113insG
ENST00000636930.2:c.2762-114_2762-113insG MANE Select	ENSP00000490491.2:n.2762-114_2762-113insG
ENST00000637810.1:c.263-114_263-113insG	ENSP00000489636.1:n.263-114_263-113insG
ENST00000637904.1:c.263-114_263-113insG	ENSP00000490550.1:n.263-114_263-113insG
ENST00000647938.1:c.2552-114_2552-113insG	ENSP00000498155.1:n.2552-114_2552-113insG
ENST00000674190.1:n.1511-114_1511-113insG
ENST00000319584.10:c.779-114_779-113insG	ENSP00000313006.6:n.779-114_779-113insG
ENST00000346085.9:c.2552-114_2552-113insG	ENSP00000344546.4:n.2552-114_2552-113insG
ENST00000350026.9:c.2513-114_2513-113insG	ENSP00000055163.7:n.2513-114_2513-113insG
ENST00000414678.6:c.920-114_920-113insG	ENSP00000412835.2:n.920-114_920-113insG
ENST00000452544.1:n.609-114_609-113insG
NM_017519.2:c.2513-114_2513-113insG	NP_059989.2:n.2513-114_2513-113insG
NM_020732.3:c.2552-114_2552-113insG	NP_065783.3:n.2552-114_2552-113insG
XM_005267069.3:c.2513-114_2513-113insG	XP_005267126.2:n.2513-114_2513-113insG
XM_011535984.1:c.1463-114_1463-113insG	XP_011534286.1:n.1463-114_1463-113insG
XM_011535985.1:c.1283-114_1283-113insG	XP_011534287.1:n.1283-114_1283-113insG
XM_011535986.1:c.1043-114_1043-113insG	XP_011534288.1:n.1043-114_1043-113insG
XM_011535987.1:c.662-114_662-113insG	XP_011534289.1:n.662-114_662-113insG
XM_011535988.1:c.-20+15303_-20+15304insG	XP_011534290.1:n.-20+15303_-20+15304insG
NM_001346813.1:c.2513-114_2513-113insG	NP_001333742.1:n.2513-114_2513-113insG
NM_001363725.1:c.263-114_263-113insG	NP_001350654.1:n.263-114_263-113insG
XM_011535984.2:c.2594-114_2594-113insG	XP_011534286.2:n.2594-114_2594-113insG
XM_011535988.3:c.-20+15303_-20+15304insG	XP_011534290.1:n.-20+15303_-20+15304insG
XM_017011103.2:c.2594-114_2594-113insG	XP_016866592.1:n.2594-114_2594-113insG
XM_017011104.1:c.2594-114_2594-113insG	XP_016866593.1:n.2594-114_2594-113insG
XM_017011105.2:c.2594-114_2594-113insG	XP_016866594.1:n.2594-114_2594-113insG
XM_017011106.2:c.2594-114_2594-113insG	XP_016866595.1:n.2594-114_2594-113insG
XM_017011107.2:c.2414-114_2414-113insG	XP_016866596.1:n.2414-114_2414-113insG
XR_002956289.1:n.2677-114_2677-113insG
NM_001363725.2:c.263-114_263-113insG	NP_001350654.1:n.263-114_263-113insG
NM_001371656.1:c.2801-114_2801-113insG	NP_001358585.1:n.2801-114_2801-113insG
NM_001374820.1:c.2801-114_2801-113insG	NP_001361749.1:n.2801-114_2801-113insG
NM_001374828.1:c.2762-114_2762-113insG MANE Select	NP_001361757.1:n.2762-114_2762-113insG
NM_017519.3:c.2762-114_2762-113insG	NP_059989.3:n.2762-114_2762-113insG