Canonical Allele Identifier: CA366234698

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157511184C>G (hg19) ; chr6:g.157190050C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157190050C>G , CM000668.2:g.157190050C>G	GRCh38
NC_000006.11:g.157511184C>G , CM000668.1:g.157511184C>G	GRCh37
NC_000006.10:g.157552876C>G	NCBI36
NG_032093.1:g.417121C>G
NG_032093.2:g.417121C>G
NG_066624.1:g.419025C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3912C>G	ENSP00000055163.8:p.Ile1304Met
ENST00000414678.8:c.3981C>G	ENSP00000412835.3:p.Ile1327Met
ENST00000637015.2:c.4200C>G	ENSP00000489729.2:p.Ile1400Met
ENST00000346085.10:c.3951C>G	ENSP00000344546.5:p.Ile1317Met
ENST00000350026.10:c.3663C>G	ENSP00000055163.7:p.Ile1221Met
ENST00000414678.7:c.2229C>G	ENSP00000412835.2:p.Ile743Met
ENST00000635849.1:c.1392C>G	ENSP00000490948.1:p.Ile464Met
ENST00000635957.1:c.1023C>G	ENSP00000490385.1:p.Ile341Met
ENST00000636930.2:c.4071C>G MANE Select	ENSP00000490491.2:p.Ile1357Met
ENST00000636940.1:n.2068C>G
ENST00000637015.1:c.1439C>G
ENST00000637568.1:c.1353C>G
ENST00000637741.1:n.737C>G
ENST00000637810.1:c.1413C>G	ENSP00000489636.1:p.Ile471Met
ENST00000637904.1:c.1572C>G	ENSP00000490550.1:p.Ile524Met
ENST00000647938.1:c.3702C>G	ENSP00000498155.1:p.Ile1234Met
ENST00000346085.9:c.3702C>G	ENSP00000344546.4:p.Ile1234Met
ENST00000350026.9:c.3663C>G	ENSP00000055163.7:p.Ile1221Met
ENST00000414678.6:c.2229C>G	ENSP00000412835.2:p.Ile743Met
NM_017519.2:c.3663C>G	NP_059989.2:p.Ile1221Met
NM_020732.3:c.3702C>G	NP_065783.3:p.Ile1234Met
XM_005267069.3:c.3822C>G	XP_005267126.2:p.Ile1274Met
XM_011535984.1:c.2901C>G	XP_011534286.1:p.Ile967Met
XM_011535985.1:c.2721C>G	XP_011534287.1:p.Ile907Met
XM_011535986.1:c.2481C>G	XP_011534288.1:p.Ile827Met
XM_011535987.1:c.2100C>G	XP_011534289.1:p.Ile700Met
XM_011535988.1:c.963C>G	XP_011534290.1:p.Ile321Met
NM_001346813.1:c.3822C>G	NP_001333742.1:p.Ile1274Met
NM_001363725.1:c.1572C>G	NP_001350654.1:p.Ile524Met
XM_011535984.2:c.4032C>G	XP_011534286.2:p.Ile1344Met
XM_011535988.3:c.963C>G	XP_011534290.1:p.Ile321Met
XM_017011103.2:c.3933C>G	XP_016866592.1:p.Ile1311Met
XM_017011104.1:c.3903C>G	XP_016866593.1:p.Ile1301Met
XM_017011105.2:c.3873C>G	XP_016866594.1:p.Ile1291Met
XM_017011106.2:c.3744C>G	XP_016866595.1:p.Ile1248Met
XM_017011107.2:c.3723C>G	XP_016866596.1:p.Ile1241Met
XR_002956289.1:n.4115C>G
NM_001363725.2:c.1572C>G	NP_001350654.1:p.Ile524Met
NM_001371656.1:c.3951C>G	NP_001358585.1:p.Ile1317Met
NM_001374820.1:c.3951C>G	NP_001361749.1:p.Ile1317Met
NM_001374828.1:c.4071C>G MANE Select	NP_001361757.1:p.Ile1357Met
NM_017519.3:c.3912C>G	NP_059989.3:p.Ile1304Met