Canonical Allele Identifier: CA366242420

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157201293-A-G
• MyVariant Identifiers: chr6:g.157522427A>G (hg19) ; chr6:g.157201293A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201293A>G , CM000668.2:g.157201293A>G	GRCh38
NC_000006.11:g.157522427A>G , CM000668.1:g.157522427A>G	GRCh37
NC_000006.10:g.157564119A>G	NCBI36
NG_032093.1:g.428364A>G
NG_032093.2:g.428364A>G
NG_066624.1:g.430268A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4909A>G	ENSP00000055163.8:p.Met1637Val
ENST00000414678.8:c.4978A>G	ENSP00000412835.3:p.Met1660Val
ENST00000637015.2:c.5197A>G	ENSP00000489729.2:p.Met1733Val
ENST00000346085.10:c.4948A>G	ENSP00000344546.5:p.Met1650Val
ENST00000350026.10:c.4660A>G	ENSP00000055163.7:p.Met1554Val
ENST00000414678.7:c.3226A>G	ENSP00000412835.2:p.Met1076Val
ENST00000635849.1:c.2389A>G	ENSP00000490948.1:p.Met797Val
ENST00000635957.1:c.2020A>G	ENSP00000490385.1:p.Met674Val
ENST00000636227.1:n.3531A>G
ENST00000636254.1:n.988A>G
ENST00000636930.2:c.5068A>G MANE Select	ENSP00000490491.2:p.Met1690Val
ENST00000636940.1:n.3065A>G
ENST00000637015.1:c.2436A>G
ENST00000637568.1:c.2350A>G
ENST00000637741.1:n.1734A>G
ENST00000637810.1:c.2410A>G	ENSP00000489636.1:p.Met804Val
ENST00000637904.1:c.2569A>G	ENSP00000490550.1:p.Met857Val
ENST00000647938.1:c.4699A>G	ENSP00000498155.1:p.Met1567Val
ENST00000346085.9:c.4699A>G	ENSP00000344546.4:p.Met1567Val
ENST00000350026.9:c.4660A>G	ENSP00000055163.7:p.Met1554Val
ENST00000414678.6:c.3226A>G	ENSP00000412835.2:p.Met1076Val
NM_017519.2:c.4660A>G	NP_059989.2:p.Met1554Val
NM_020732.3:c.4699A>G	NP_065783.3:p.Met1567Val
XM_005267069.3:c.4819A>G	XP_005267126.2:p.Met1607Val
XM_011535984.1:c.3898A>G	XP_011534286.1:p.Met1300Val
XM_011535985.1:c.3718A>G	XP_011534287.1:p.Met1240Val
XM_011535986.1:c.3478A>G	XP_011534288.1:p.Met1160Val
XM_011535987.1:c.3097A>G	XP_011534289.1:p.Met1033Val
XM_011535988.1:c.1960A>G	XP_011534290.1:p.Met654Val
NM_001346813.1:c.4819A>G	NP_001333742.1:p.Met1607Val
NM_001363725.1:c.2569A>G	NP_001350654.1:p.Met857Val
XM_011535984.2:c.5029A>G	XP_011534286.2:p.Met1677Val
XM_011535988.3:c.1960A>G	XP_011534290.1:p.Met654Val
XM_017011103.2:c.4930A>G	XP_016866592.1:p.Met1644Val
XM_017011104.1:c.4900A>G	XP_016866593.1:p.Met1634Val
XM_017011105.2:c.4870A>G	XP_016866594.1:p.Met1624Val
XM_017011106.2:c.4741A>G	XP_016866595.1:p.Met1581Val
XM_017011107.2:c.4720A>G	XP_016866596.1:p.Met1574Val
XR_002956289.1:n.5015A>G
NM_001363725.2:c.2569A>G	NP_001350654.1:p.Met857Val
NM_001371656.1:c.4948A>G	NP_001358585.1:p.Met1650Val
NM_001374820.1:c.4948A>G	NP_001361749.1:p.Met1650Val
NM_001374828.1:c.5068A>G MANE Select	NP_001361757.1:p.Met1690Val
NM_017519.3:c.4909A>G	NP_059989.3:p.Met1637Val