Canonical Allele Identifier: CA2713412265

Gene: ARID1B

Linked Data

• dbSNP Id: rs2128211308

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156901583_156901584insGCTGG , CM000668.2:g.156901583_156901584insGCTGG	GRCh38
NC_000006.11:g.157222717_157222718insGCTGG , CM000668.1:g.157222717_157222718insGCTGG	GRCh37
NC_000006.10:g.157264409_157264410insGCTGG	NCBI36
NG_032093.1:g.128654_128655insGCTGG
NG_032093.2:g.128654_128655insGCTGG
NG_066624.1:g.130558_130559insGCTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2136+58_2136+59insGCTGG	ENSP00000055163.8:n.2136+58_2136+59insGCTGG
ENST00000414678.8:c.2136+58_2136+59insGCTGG	ENSP00000412835.3:n.2136+58_2136+59insGCTGG
ENST00000637015.2:c.2136+58_2136+59insGCTGG	ENSP00000489729.2:n.2136+58_2136+59insGCTGG
ENST00000319584.11:c.150+58_150+59insGCTGG	ENSP00000313006.7:n.150+58_150+59insGCTGG
ENST00000346085.10:c.2175+58_2175+59insGCTGG	ENSP00000344546.5:n.2175+58_2175+59insGCTGG
ENST00000350026.10:c.1887+58_1887+59insGCTGG	ENSP00000055163.7:n.1887+58_1887+59insGCTGG
ENST00000414678.7:c.384+58_384+59insGCTGG	ENSP00000412835.2:n.384+58_384+59insGCTGG
ENST00000636205.1:n.257_258insGCTGG
ENST00000636748.1:c.417+58_417+59insGCTGG	ENSP00000489917.1:n.417+58_417+59insGCTGG
ENST00000636930.2:c.2136+58_2136+59insGCTGG MANE Select	ENSP00000490491.2:n.2136+58_2136+59insGCTGG
ENST00000637532.1:c.162+58_162+59insGCTGG	ENSP00000490420.1:n.162+58_162+59insGCTGG
ENST00000638000.1:c.353+58_353+59insGCTGG
ENST00000647938.1:c.1926+58_1926+59insGCTGG	ENSP00000498155.1:n.1926+58_1926+59insGCTGG
ENST00000674190.1:n.843+58_843+59insGCTGG
ENST00000674298.1:c.1876+58_1876+59insGCTGG
ENST00000319584.10:c.153+58_153+59insGCTGG	ENSP00000313006.6:n.153+58_153+59insGCTGG
ENST00000346085.9:c.1926+58_1926+59insGCTGG	ENSP00000344546.4:n.1926+58_1926+59insGCTGG
ENST00000350026.9:c.1887+58_1887+59insGCTGG	ENSP00000055163.7:n.1887+58_1887+59insGCTGG
ENST00000414678.6:c.384+58_384+59insGCTGG	ENSP00000412835.2:n.384+58_384+59insGCTGG
NM_017519.2:c.1887+58_1887+59insGCTGG	NP_059989.2:n.1887+58_1887+59insGCTGG
NM_020732.3:c.1926+58_1926+59insGCTGG	NP_065783.3:n.1926+58_1926+59insGCTGG
XM_005267069.3:c.1887+58_1887+59insGCTGG	XP_005267126.2:n.1887+58_1887+59insGCTGG
XM_011535984.1:c.795+58_795+59insGCTGG	XP_011534286.1:n.795+58_795+59insGCTGG
XM_011535985.1:c.795+58_795+59insGCTGG	XP_011534287.1:n.795+58_795+59insGCTGG
XM_011535986.1:c.375+58_375+59insGCTGG	XP_011534288.1:n.375+58_375+59insGCTGG
NM_001346813.1:c.1887+58_1887+59insGCTGG	NP_001333742.1:n.1887+58_1887+59insGCTGG
XM_011535984.2:c.1926+58_1926+59insGCTGG	XP_011534286.2:n.1926+58_1926+59insGCTGG
XM_017011103.2:c.1926+58_1926+59insGCTGG	XP_016866592.1:n.1926+58_1926+59insGCTGG
XM_017011104.1:c.1926+58_1926+59insGCTGG	XP_016866593.1:n.1926+58_1926+59insGCTGG
XM_017011105.2:c.1926+58_1926+59insGCTGG	XP_016866594.1:n.1926+58_1926+59insGCTGG
XM_017011106.2:c.1926+58_1926+59insGCTGG	XP_016866595.1:n.1926+58_1926+59insGCTGG
XM_017011107.2:c.1926+58_1926+59insGCTGG	XP_016866596.1:n.1926+58_1926+59insGCTGG
XR_002956289.1:n.2009+58_2009+59insGCTGG
NM_001371656.1:c.2175+58_2175+59insGCTGG	NP_001358585.1:n.2175+58_2175+59insGCTGG
NM_001374820.1:c.2175+58_2175+59insGCTGG	NP_001361749.1:n.2175+58_2175+59insGCTGG
NM_001374828.1:c.2136+58_2136+59insGCTGG MANE Select	NP_001361757.1:n.2136+58_2136+59insGCTGG
NM_017519.3:c.2136+58_2136+59insGCTGG	NP_059989.3:n.2136+58_2136+59insGCTGG