Canonical Allele Identifier: CA366235310

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511253C>G (hg19) ; chr6:g.157190119C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190119C>G , CM000668.2:g.157190119C>G	GRCh38
NC_000006.11:g.157511253C>G , CM000668.1:g.157511253C>G	GRCh37
NC_000006.10:g.157552945C>G	NCBI36
NG_032093.1:g.417190C>G
NG_032093.2:g.417190C>G
NG_066624.1:g.419094C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3981C>G	ENSP00000055163.8:p.Asn1327Lys
ENST00000414678.8:c.4050C>G	ENSP00000412835.3:p.Asn1350Lys
ENST00000637015.2:c.4269C>G	ENSP00000489729.2:p.Asn1423Lys
ENST00000346085.10:c.4020C>G	ENSP00000344546.5:p.Asn1340Lys
ENST00000350026.10:c.3732C>G	ENSP00000055163.7:p.Asn1244Lys
ENST00000414678.7:c.2298C>G	ENSP00000412835.2:p.Asn766Lys
ENST00000635849.1:c.1461C>G	ENSP00000490948.1:p.Asn487Lys
ENST00000635957.1:c.1092C>G	ENSP00000490385.1:p.Asn364Lys
ENST00000636930.2:c.4140C>G MANE Select	ENSP00000490491.2:p.Asn1380Lys
ENST00000636940.1:n.2137C>G
ENST00000637015.1:c.1508C>G
ENST00000637568.1:c.1422C>G
ENST00000637741.1:n.806C>G
ENST00000637810.1:c.1482C>G	ENSP00000489636.1:p.Asn494Lys
ENST00000637904.1:c.1641C>G	ENSP00000490550.1:p.Asn547Lys
ENST00000647938.1:c.3771C>G	ENSP00000498155.1:p.Asn1257Lys
ENST00000346085.9:c.3771C>G	ENSP00000344546.4:p.Asn1257Lys
ENST00000350026.9:c.3732C>G	ENSP00000055163.7:p.Asn1244Lys
ENST00000414678.6:c.2298C>G	ENSP00000412835.2:p.Asn766Lys
NM_017519.2:c.3732C>G	NP_059989.2:p.Asn1244Lys
NM_020732.3:c.3771C>G	NP_065783.3:p.Asn1257Lys
XM_005267069.3:c.3891C>G	XP_005267126.2:p.Asn1297Lys
XM_011535984.1:c.2970C>G	XP_011534286.1:p.Asn990Lys
XM_011535985.1:c.2790C>G	XP_011534287.1:p.Asn930Lys
XM_011535986.1:c.2550C>G	XP_011534288.1:p.Asn850Lys
XM_011535987.1:c.2169C>G	XP_011534289.1:p.Asn723Lys
XM_011535988.1:c.1032C>G	XP_011534290.1:p.Asn344Lys
NM_001346813.1:c.3891C>G	NP_001333742.1:p.Asn1297Lys
NM_001363725.1:c.1641C>G	NP_001350654.1:p.Asn547Lys
XM_011535984.2:c.4101C>G	XP_011534286.2:p.Asn1367Lys
XM_011535988.3:c.1032C>G	XP_011534290.1:p.Asn344Lys
XM_017011103.2:c.4002C>G	XP_016866592.1:p.Asn1334Lys
XM_017011104.1:c.3972C>G	XP_016866593.1:p.Asn1324Lys
XM_017011105.2:c.3942C>G	XP_016866594.1:p.Asn1314Lys
XM_017011106.2:c.3813C>G	XP_016866595.1:p.Asn1271Lys
XM_017011107.2:c.3792C>G	XP_016866596.1:p.Asn1264Lys
XR_002956289.1:n.4184C>G
NM_001363725.2:c.1641C>G	NP_001350654.1:p.Asn547Lys
NM_001371656.1:c.4020C>G	NP_001358585.1:p.Asn1340Lys
NM_001374820.1:c.4020C>G	NP_001361749.1:p.Asn1340Lys
NM_001374828.1:c.4140C>G MANE Select	NP_001361757.1:p.Asn1380Lys
NM_017519.3:c.3981C>G	NP_059989.3:p.Asn1327Lys