Canonical Allele Identifier: CA366389272

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157148933-C-G
• MyVariant Identifiers: chr6:g.157470067C>G (hg19) ; chr6:g.157148933C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148933C>G , CM000668.2:g.157148933C>G	GRCh38
NC_000006.11:g.157470067C>G , CM000668.1:g.157470067C>G	GRCh37
NC_000006.10:g.157511759C>G	NCBI36
NG_032093.1:g.376004C>G
NG_032093.2:g.376004C>G
NG_066624.1:g.377908C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3071C>G	ENSP00000055163.8:p.Ala1024Gly
ENST00000414678.8:c.2981C>G	ENSP00000412835.3:p.Ala994Gly
ENST00000637015.2:c.3071C>G	ENSP00000489729.2:p.Ala1024Gly
ENST00000319584.11:c.1085C>G	ENSP00000313006.7:p.Ala362Gly
ENST00000346085.10:c.3110C>G	ENSP00000344546.5:p.Ala1037Gly
ENST00000350026.10:c.2822C>G	ENSP00000055163.7:p.Ala941Gly
ENST00000414678.7:c.1229C>G	ENSP00000412835.2:p.Ala410Gly
ENST00000452544.2:n.972C>G
ENST00000635849.1:c.392C>G	ENSP00000490948.1:p.Ala131Gly
ENST00000635957.1:c.26C>G	ENSP00000490385.1:p.Ala9Gly
ENST00000636426.1:n.205C>G
ENST00000636930.2:c.3071C>G MANE Select	ENSP00000490491.2:p.Ala1024Gly
ENST00000637015.1:c.310C>G
ENST00000637568.1:c.114C>G
ENST00000637810.1:c.572C>G	ENSP00000489636.1:p.Ala191Gly
ENST00000637904.1:c.572C>G	ENSP00000490550.1:p.Ala191Gly
ENST00000647938.1:c.2861C>G	ENSP00000498155.1:p.Ala954Gly
ENST00000674190.1:n.1820C>G
ENST00000319584.10:c.1088C>G	ENSP00000313006.6:p.Ala363Gly
ENST00000346085.9:c.2861C>G	ENSP00000344546.4:p.Ala954Gly
ENST00000350026.9:c.2822C>G	ENSP00000055163.7:p.Ala941Gly
ENST00000400790.3:c.23C>G	ENSP00000383596.3:p.Ala8Gly
ENST00000414678.6:c.1229C>G	ENSP00000412835.2:p.Ala410Gly
ENST00000452544.1:n.918C>G
ENST00000478761.3:c.144C>G
NM_017519.2:c.2822C>G	NP_059989.2:p.Ala941Gly
NM_020732.3:c.2861C>G	NP_065783.3:p.Ala954Gly
XM_005267069.3:c.2822C>G	XP_005267126.2:p.Ala941Gly
XM_011535984.1:c.1772C>G	XP_011534286.1:p.Ala591Gly
XM_011535985.1:c.1592C>G	XP_011534287.1:p.Ala531Gly
XM_011535986.1:c.1352C>G	XP_011534288.1:p.Ala451Gly
XM_011535987.1:c.971C>G	XP_011534289.1:p.Ala324Gly
XM_011535988.1:c.-20+15726C>G	XP_011534290.1:n.-20+15726C>G
NM_001346813.1:c.2822C>G	NP_001333742.1:p.Ala941Gly
NM_001363725.1:c.572C>G	NP_001350654.1:p.Ala191Gly
XM_011535984.2:c.2903C>G	XP_011534286.2:p.Ala968Gly
XM_011535988.3:c.-20+15726C>G	XP_011534290.1:n.-20+15726C>G
XM_017011103.2:c.2903C>G	XP_016866592.1:p.Ala968Gly
XM_017011104.1:c.2903C>G	XP_016866593.1:p.Ala968Gly
XM_017011105.2:c.2903C>G	XP_016866594.1:p.Ala968Gly
XM_017011106.2:c.2903C>G	XP_016866595.1:p.Ala968Gly
XM_017011107.2:c.2723C>G	XP_016866596.1:p.Ala908Gly
XR_002956289.1:n.2986C>G
NM_001363725.2:c.572C>G	NP_001350654.1:p.Ala191Gly
NM_001371656.1:c.3110C>G	NP_001358585.1:p.Ala1037Gly
NM_001374820.1:c.3110C>G	NP_001361749.1:p.Ala1037Gly
NM_001374828.1:c.3071C>G MANE Select	NP_001361757.1:p.Ala1024Gly
NM_017519.3:c.3071C>G	NP_059989.3:p.Ala1024Gly