Canonical Allele Identifier: CA366234060

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157189674-C-G
• MyVariant Identifiers: chr6:g.157510808C>G (hg19) ; chr6:g.157189674C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157189674C>G , CM000668.2:g.157189674C>G	GRCh38
NC_000006.11:g.157510808C>G , CM000668.1:g.157510808C>G	GRCh37
NC_000006.10:g.157552500C>G	NCBI36
NG_032093.1:g.416745C>G
NG_032093.2:g.416745C>G
NG_066624.1:g.418649C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3793C>G	ENSP00000055163.8:p.Pro1265Ala
ENST00000414678.8:c.3862C>G	ENSP00000412835.3:p.Pro1288Ala
ENST00000637015.2:c.4081C>G	ENSP00000489729.2:p.Pro1361Ala
ENST00000346085.10:c.3832C>G	ENSP00000344546.5:p.Pro1278Ala
ENST00000350026.10:c.3544C>G	ENSP00000055163.7:p.Pro1182Ala
ENST00000414678.7:c.2110C>G	ENSP00000412835.2:p.Pro704Ala
ENST00000635849.1:c.1273C>G	ENSP00000490948.1:p.Pro425Ala
ENST00000635957.1:c.907C>G	ENSP00000490385.1:p.Pro303Ala
ENST00000636930.2:c.3952C>G MANE Select	ENSP00000490491.2:p.Pro1318Ala
ENST00000636940.1:n.1949C>G
ENST00000637015.1:c.1320C>G
ENST00000637568.1:c.1234C>G
ENST00000637741.1:n.618C>G
ENST00000637810.1:c.1294C>G	ENSP00000489636.1:p.Pro432Ala
ENST00000637904.1:c.1453C>G	ENSP00000490550.1:p.Pro485Ala
ENST00000647938.1:c.3583C>G	ENSP00000498155.1:p.Pro1195Ala
ENST00000346085.9:c.3583C>G	ENSP00000344546.4:p.Pro1195Ala
ENST00000350026.9:c.3544C>G	ENSP00000055163.7:p.Pro1182Ala
ENST00000414678.6:c.2110C>G	ENSP00000412835.2:p.Pro704Ala
NM_017519.2:c.3544C>G	NP_059989.2:p.Pro1182Ala
NM_020732.3:c.3583C>G	NP_065783.3:p.Pro1195Ala
XM_005267069.3:c.3703C>G	XP_005267126.2:p.Pro1235Ala
XM_011535984.1:c.2782C>G	XP_011534286.1:p.Pro928Ala
XM_011535985.1:c.2602C>G	XP_011534287.1:p.Pro868Ala
XM_011535986.1:c.2362C>G	XP_011534288.1:p.Pro788Ala
XM_011535987.1:c.1981C>G	XP_011534289.1:p.Pro661Ala
XM_011535988.1:c.844C>G	XP_011534290.1:p.Pro282Ala
NM_001346813.1:c.3703C>G	NP_001333742.1:p.Pro1235Ala
NM_001363725.1:c.1453C>G	NP_001350654.1:p.Pro485Ala
XM_011535984.2:c.3913C>G	XP_011534286.2:p.Pro1305Ala
XM_011535988.3:c.844C>G	XP_011534290.1:p.Pro282Ala
XM_017011103.2:c.3814C>G	XP_016866592.1:p.Pro1272Ala
XM_017011104.1:c.3784C>G	XP_016866593.1:p.Pro1262Ala
XM_017011105.2:c.3754C>G	XP_016866594.1:p.Pro1252Ala
XM_017011106.2:c.3625C>G	XP_016866595.1:p.Pro1209Ala
XM_017011107.2:c.3604C>G	XP_016866596.1:p.Pro1202Ala
XR_002956289.1:n.3996C>G
NM_001363725.2:c.1453C>G	NP_001350654.1:p.Pro485Ala
NM_001371656.1:c.3832C>G	NP_001358585.1:p.Pro1278Ala
NM_001374820.1:c.3832C>G	NP_001361749.1:p.Pro1278Ala
NM_001374828.1:c.3952C>G MANE Select	NP_001361757.1:p.Pro1318Ala
NM_017519.3:c.3793C>G	NP_059989.3:p.Pro1265Ala