Canonical Allele Identifier: CA366388890

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157469890C>A (hg19) ; chr6:g.157148756C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148756C>A , CM000668.2:g.157148756C>A	GRCh38
NC_000006.11:g.157469890C>A , CM000668.1:g.157469890C>A	GRCh37
NC_000006.10:g.157511582C>A	NCBI36
NG_032093.1:g.375827C>A
NG_032093.2:g.375827C>A
NG_066624.1:g.377731C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.2894C>A	ENSP00000055163.8:p.Pro965His
ENST00000414678.8:c.2804C>A	ENSP00000412835.3:p.Pro935His
ENST00000637015.2:c.2894C>A	ENSP00000489729.2:p.Pro965His
ENST00000319584.11:c.908C>A	ENSP00000313006.7:p.Pro303His
ENST00000346085.10:c.2933C>A	ENSP00000344546.5:p.Pro978His
ENST00000350026.10:c.2645C>A	ENSP00000055163.7:p.Pro882His
ENST00000414678.7:c.1052C>A	ENSP00000412835.2:p.Pro351His
ENST00000452544.2:n.795C>A
ENST00000635849.1:c.215C>A	ENSP00000490948.1:p.Pro72His
ENST00000636426.1:n.28C>A
ENST00000636930.2:c.2894C>A MANE Select	ENSP00000490491.2:p.Pro965His
ENST00000637015.1:c.133C>A
ENST00000637810.1:c.395C>A	ENSP00000489636.1:p.Pro132His
ENST00000637904.1:c.395C>A	ENSP00000490550.1:p.Pro132His
ENST00000647938.1:c.2684C>A	ENSP00000498155.1:p.Pro895His
ENST00000674190.1:n.1643C>A
ENST00000319584.10:c.911C>A	ENSP00000313006.6:p.Pro304His
ENST00000346085.9:c.2684C>A	ENSP00000344546.4:p.Pro895His
ENST00000350026.9:c.2645C>A	ENSP00000055163.7:p.Pro882His
ENST00000414678.6:c.1052C>A	ENSP00000412835.2:p.Pro351His
ENST00000452544.1:n.741C>A
NM_017519.2:c.2645C>A	NP_059989.2:p.Pro882His
NM_020732.3:c.2684C>A	NP_065783.3:p.Pro895His
XM_005267069.3:c.2645C>A	XP_005267126.2:p.Pro882His
XM_011535984.1:c.1595C>A	XP_011534286.1:p.Pro532His
XM_011535985.1:c.1415C>A	XP_011534287.1:p.Pro472His
XM_011535986.1:c.1175C>A	XP_011534288.1:p.Pro392His
XM_011535987.1:c.794C>A	XP_011534289.1:p.Pro265His
XM_011535988.1:c.-20+15549C>A	XP_011534290.1:n.-20+15549C>A
NM_001346813.1:c.2645C>A	NP_001333742.1:p.Pro882His
NM_001363725.1:c.395C>A	NP_001350654.1:p.Pro132His
XM_011535984.2:c.2726C>A	XP_011534286.2:p.Pro909His
XM_011535988.3:c.-20+15549C>A	XP_011534290.1:n.-20+15549C>A
XM_017011103.2:c.2726C>A	XP_016866592.1:p.Pro909His
XM_017011104.1:c.2726C>A	XP_016866593.1:p.Pro909His
XM_017011105.2:c.2726C>A	XP_016866594.1:p.Pro909His
XM_017011106.2:c.2726C>A	XP_016866595.1:p.Pro909His
XM_017011107.2:c.2546C>A	XP_016866596.1:p.Pro849His
XR_002956289.1:n.2809C>A
NM_001363725.2:c.395C>A	NP_001350654.1:p.Pro132His
NM_001371656.1:c.2933C>A	NP_001358585.1:p.Pro978His
NM_001374820.1:c.2933C>A	NP_001361749.1:p.Pro978His
NM_001374828.1:c.2894C>A MANE Select	NP_001361757.1:p.Pro965His
NM_017519.3:c.2894C>A	NP_059989.3:p.Pro965His