Canonical Allele Identifier: CA366389112

Gene: ARID1B

Linked Data

• gnomAD v4: 6-157148858-C-G
• MyVariant Identifiers: chr6:g.157469992C>G (hg19) ; chr6:g.157148858C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148858C>G , CM000668.2:g.157148858C>G	GRCh38
NC_000006.11:g.157469992C>G , CM000668.1:g.157469992C>G	GRCh37
NC_000006.10:g.157511684C>G	NCBI36
NG_032093.1:g.375929C>G
NG_032093.2:g.375929C>G
NG_066624.1:g.377833C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.2996C>G	ENSP00000055163.8:p.Pro999Arg
ENST00000414678.8:c.2906C>G	ENSP00000412835.3:p.Pro969Arg
ENST00000637015.2:c.2996C>G	ENSP00000489729.2:p.Pro999Arg
ENST00000319584.11:c.1010C>G	ENSP00000313006.7:p.Pro337Arg
ENST00000346085.10:c.3035C>G	ENSP00000344546.5:p.Pro1012Arg
ENST00000350026.10:c.2747C>G	ENSP00000055163.7:p.Pro916Arg
ENST00000414678.7:c.1154C>G	ENSP00000412835.2:p.Pro385Arg
ENST00000452544.2:n.897C>G
ENST00000635849.1:c.317C>G	ENSP00000490948.1:p.Pro106Arg
ENST00000636426.1:n.130C>G
ENST00000636930.2:c.2996C>G MANE Select	ENSP00000490491.2:p.Pro999Arg
ENST00000637015.1:c.235C>G
ENST00000637568.1:c.39C>G
ENST00000637810.1:c.497C>G	ENSP00000489636.1:p.Pro166Arg
ENST00000637904.1:c.497C>G	ENSP00000490550.1:p.Pro166Arg
ENST00000647938.1:c.2786C>G	ENSP00000498155.1:p.Pro929Arg
ENST00000674190.1:n.1745C>G
ENST00000319584.10:c.1013C>G	ENSP00000313006.6:p.Pro338Arg
ENST00000346085.9:c.2786C>G	ENSP00000344546.4:p.Pro929Arg
ENST00000350026.9:c.2747C>G	ENSP00000055163.7:p.Pro916Arg
ENST00000414678.6:c.1154C>G	ENSP00000412835.2:p.Pro385Arg
ENST00000452544.1:n.843C>G
ENST00000478761.3:c.69C>G
NM_017519.2:c.2747C>G	NP_059989.2:p.Pro916Arg
NM_020732.3:c.2786C>G	NP_065783.3:p.Pro929Arg
XM_005267069.3:c.2747C>G	XP_005267126.2:p.Pro916Arg
XM_011535984.1:c.1697C>G	XP_011534286.1:p.Pro566Arg
XM_011535985.1:c.1517C>G	XP_011534287.1:p.Pro506Arg
XM_011535986.1:c.1277C>G	XP_011534288.1:p.Pro426Arg
XM_011535987.1:c.896C>G	XP_011534289.1:p.Pro299Arg
XM_011535988.1:c.-20+15651C>G	XP_011534290.1:n.-20+15651C>G
NM_001346813.1:c.2747C>G	NP_001333742.1:p.Pro916Arg
NM_001363725.1:c.497C>G	NP_001350654.1:p.Pro166Arg
XM_011535984.2:c.2828C>G	XP_011534286.2:p.Pro943Arg
XM_011535988.3:c.-20+15651C>G	XP_011534290.1:n.-20+15651C>G
XM_017011103.2:c.2828C>G	XP_016866592.1:p.Pro943Arg
XM_017011104.1:c.2828C>G	XP_016866593.1:p.Pro943Arg
XM_017011105.2:c.2828C>G	XP_016866594.1:p.Pro943Arg
XM_017011106.2:c.2828C>G	XP_016866595.1:p.Pro943Arg
XM_017011107.2:c.2648C>G	XP_016866596.1:p.Pro883Arg
XR_002956289.1:n.2911C>G
NM_001363725.2:c.497C>G	NP_001350654.1:p.Pro166Arg
NM_001371656.1:c.3035C>G	NP_001358585.1:p.Pro1012Arg
NM_001374820.1:c.3035C>G	NP_001361749.1:p.Pro1012Arg
NM_001374828.1:c.2996C>G MANE Select	NP_001361757.1:p.Pro999Arg
NM_017519.3:c.2996C>G	NP_059989.3:p.Pro999Arg