Canonical Allele Identifier: CA452990350

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157148859-A-G
• MyVariant Identifiers: chr6:g.157469993A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148859A>G , CM000668.2:g.157148859A>G	GRCh38
NC_000006.11:g.157469993A>G , CM000668.1:g.157469993A>G	GRCh37
NC_000006.10:g.157511685A>G	NCBI36
NG_032093.1:g.375930A>G
NG_032093.2:g.375930A>G
NG_066624.1:g.377834A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.2997A>G	ENSP00000055163.8:p.Pro999=
ENST00000414678.8:c.2907A>G	ENSP00000412835.3:p.Pro969=
ENST00000637015.2:c.2997A>G	ENSP00000489729.2:p.Pro999=
ENST00000319584.11:c.1011A>G	ENSP00000313006.7:p.Pro337=
ENST00000346085.10:c.3036A>G	ENSP00000344546.5:p.Pro1012=
ENST00000350026.10:c.2748A>G	ENSP00000055163.7:p.Pro916=
ENST00000414678.7:c.1155A>G	ENSP00000412835.2:p.Pro385=
ENST00000452544.2:n.898A>G
ENST00000635849.1:c.318A>G	ENSP00000490948.1:p.Pro106=
ENST00000636426.1:n.131A>G
ENST00000636930.2:c.2997A>G MANE Select	ENSP00000490491.2:p.Pro999=
ENST00000637015.1:c.236A>G
ENST00000637568.1:c.40A>G
ENST00000637810.1:c.498A>G	ENSP00000489636.1:p.Pro166=
ENST00000637904.1:c.498A>G	ENSP00000490550.1:p.Pro166=
ENST00000647938.1:c.2787A>G	ENSP00000498155.1:p.Pro929=
ENST00000674190.1:n.1746A>G
ENST00000319584.10:c.1014A>G	ENSP00000313006.6:p.Pro338=
ENST00000346085.9:c.2787A>G	ENSP00000344546.4:p.Pro929=
ENST00000350026.9:c.2748A>G	ENSP00000055163.7:p.Pro916=
ENST00000414678.6:c.1155A>G	ENSP00000412835.2:p.Pro385=
ENST00000452544.1:n.844A>G
ENST00000478761.3:c.70A>G
NM_017519.2:c.2748A>G	NP_059989.2:p.Pro916=
NM_020732.3:c.2787A>G	NP_065783.3:p.Pro929=
XM_005267069.3:c.2748A>G	XP_005267126.2:p.Pro916=
XM_011535984.1:c.1698A>G	XP_011534286.1:p.Pro566=
XM_011535985.1:c.1518A>G	XP_011534287.1:p.Pro506=
XM_011535986.1:c.1278A>G	XP_011534288.1:p.Pro426=
XM_011535987.1:c.897A>G	XP_011534289.1:p.Pro299=
XM_011535988.1:c.-20+15652A>G	XP_011534290.1:n.-20+15652A>G
NM_001346813.1:c.2748A>G	NP_001333742.1:p.Pro916=
NM_001363725.1:c.498A>G	NP_001350654.1:p.Pro166=
XM_011535984.2:c.2829A>G	XP_011534286.2:p.Pro943=
XM_011535988.3:c.-20+15652A>G	XP_011534290.1:n.-20+15652A>G
XM_017011103.2:c.2829A>G	XP_016866592.1:p.Pro943=
XM_017011104.1:c.2829A>G	XP_016866593.1:p.Pro943=
XM_017011105.2:c.2829A>G	XP_016866594.1:p.Pro943=
XM_017011106.2:c.2829A>G	XP_016866595.1:p.Pro943=
XM_017011107.2:c.2649A>G	XP_016866596.1:p.Pro883=
XR_002956289.1:n.2912A>G
NM_001363725.2:c.498A>G	NP_001350654.1:p.Pro166=
NM_001371656.1:c.3036A>G	NP_001358585.1:p.Pro1012=
NM_001374820.1:c.3036A>G	NP_001361749.1:p.Pro1012=
NM_001374828.1:c.2997A>G MANE Select	NP_001361757.1:p.Pro999=
NM_017519.3:c.2997A>G	NP_059989.3:p.Pro999=