Canonical Allele Identifier: CA366389157

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470013C>G (hg19) ; chr6:g.157148879C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148879C>G , CM000668.2:g.157148879C>G	GRCh38
NC_000006.11:g.157470013C>G , CM000668.1:g.157470013C>G	GRCh37
NC_000006.10:g.157511705C>G	NCBI36
NG_032093.1:g.375950C>G
NG_032093.2:g.375950C>G
NG_066624.1:g.377854C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3017C>G	ENSP00000055163.8:p.Pro1006Arg
ENST00000414678.8:c.2927C>G	ENSP00000412835.3:p.Pro976Arg
ENST00000637015.2:c.3017C>G	ENSP00000489729.2:p.Pro1006Arg
ENST00000319584.11:c.1031C>G	ENSP00000313006.7:p.Pro344Arg
ENST00000346085.10:c.3056C>G	ENSP00000344546.5:p.Pro1019Arg
ENST00000350026.10:c.2768C>G	ENSP00000055163.7:p.Pro923Arg
ENST00000414678.7:c.1175C>G	ENSP00000412835.2:p.Pro392Arg
ENST00000452544.2:n.918C>G
ENST00000635849.1:c.338C>G	ENSP00000490948.1:p.Pro113Arg
ENST00000636426.1:n.151C>G
ENST00000636930.2:c.3017C>G MANE Select	ENSP00000490491.2:p.Pro1006Arg
ENST00000637015.1:c.256C>G
ENST00000637568.1:c.60C>G
ENST00000637810.1:c.518C>G	ENSP00000489636.1:p.Pro173Arg
ENST00000637904.1:c.518C>G	ENSP00000490550.1:p.Pro173Arg
ENST00000647938.1:c.2807C>G	ENSP00000498155.1:p.Pro936Arg
ENST00000674190.1:n.1766C>G
ENST00000319584.10:c.1034C>G	ENSP00000313006.6:p.Pro345Arg
ENST00000346085.9:c.2807C>G	ENSP00000344546.4:p.Pro936Arg
ENST00000350026.9:c.2768C>G	ENSP00000055163.7:p.Pro923Arg
ENST00000414678.6:c.1175C>G	ENSP00000412835.2:p.Pro392Arg
ENST00000452544.1:n.864C>G
ENST00000478761.3:c.90C>G
NM_017519.2:c.2768C>G	NP_059989.2:p.Pro923Arg
NM_020732.3:c.2807C>G	NP_065783.3:p.Pro936Arg
XM_005267069.3:c.2768C>G	XP_005267126.2:p.Pro923Arg
XM_011535984.1:c.1718C>G	XP_011534286.1:p.Pro573Arg
XM_011535985.1:c.1538C>G	XP_011534287.1:p.Pro513Arg
XM_011535986.1:c.1298C>G	XP_011534288.1:p.Pro433Arg
XM_011535987.1:c.917C>G	XP_011534289.1:p.Pro306Arg
XM_011535988.1:c.-20+15672C>G	XP_011534290.1:n.-20+15672C>G
NM_001346813.1:c.2768C>G	NP_001333742.1:p.Pro923Arg
NM_001363725.1:c.518C>G	NP_001350654.1:p.Pro173Arg
XM_011535984.2:c.2849C>G	XP_011534286.2:p.Pro950Arg
XM_011535988.3:c.-20+15672C>G	XP_011534290.1:n.-20+15672C>G
XM_017011103.2:c.2849C>G	XP_016866592.1:p.Pro950Arg
XM_017011104.1:c.2849C>G	XP_016866593.1:p.Pro950Arg
XM_017011105.2:c.2849C>G	XP_016866594.1:p.Pro950Arg
XM_017011106.2:c.2849C>G	XP_016866595.1:p.Pro950Arg
XM_017011107.2:c.2669C>G	XP_016866596.1:p.Pro890Arg
XR_002956289.1:n.2932C>G
NM_001363725.2:c.518C>G	NP_001350654.1:p.Pro173Arg
NM_001371656.1:c.3056C>G	NP_001358585.1:p.Pro1019Arg
NM_001374820.1:c.3056C>G	NP_001361749.1:p.Pro1019Arg
NM_001374828.1:c.3017C>G MANE Select	NP_001361757.1:p.Pro1006Arg
NM_017519.3:c.3017C>G	NP_059989.3:p.Pro1006Arg