Canonical Allele Identifier: CA366389260

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157470061C>A (hg19) ; chr6:g.157148927C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148927C>A , CM000668.2:g.157148927C>A	GRCh38
NC_000006.11:g.157470061C>A , CM000668.1:g.157470061C>A	GRCh37
NC_000006.10:g.157511753C>A	NCBI36
NG_032093.1:g.375998C>A
NG_032093.2:g.375998C>A
NG_066624.1:g.377902C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3065C>A	ENSP00000055163.8:p.Ala1022Asp
ENST00000414678.8:c.2975C>A	ENSP00000412835.3:p.Ala992Asp
ENST00000637015.2:c.3065C>A	ENSP00000489729.2:p.Ala1022Asp
ENST00000319584.11:c.1079C>A	ENSP00000313006.7:p.Ala360Asp
ENST00000346085.10:c.3104C>A	ENSP00000344546.5:p.Ala1035Asp
ENST00000350026.10:c.2816C>A	ENSP00000055163.7:p.Ala939Asp
ENST00000414678.7:c.1223C>A	ENSP00000412835.2:p.Ala408Asp
ENST00000452544.2:n.966C>A
ENST00000635849.1:c.386C>A	ENSP00000490948.1:p.Ala129Asp
ENST00000635957.1:c.20C>A	ENSP00000490385.1:p.Ala7Asp
ENST00000636426.1:n.199C>A
ENST00000636930.2:c.3065C>A MANE Select	ENSP00000490491.2:p.Ala1022Asp
ENST00000637015.1:c.304C>A
ENST00000637568.1:c.108C>A
ENST00000637810.1:c.566C>A	ENSP00000489636.1:p.Ala189Asp
ENST00000637904.1:c.566C>A	ENSP00000490550.1:p.Ala189Asp
ENST00000647938.1:c.2855C>A	ENSP00000498155.1:p.Ala952Asp
ENST00000674190.1:n.1814C>A
ENST00000319584.10:c.1082C>A	ENSP00000313006.6:p.Ala361Asp
ENST00000346085.9:c.2855C>A	ENSP00000344546.4:p.Ala952Asp
ENST00000350026.9:c.2816C>A	ENSP00000055163.7:p.Ala939Asp
ENST00000400790.3:c.17C>A	ENSP00000383596.3:p.Ala6Asp
ENST00000414678.6:c.1223C>A	ENSP00000412835.2:p.Ala408Asp
ENST00000452544.1:n.912C>A
ENST00000478761.3:c.138C>A
NM_017519.2:c.2816C>A	NP_059989.2:p.Ala939Asp
NM_020732.3:c.2855C>A	NP_065783.3:p.Ala952Asp
XM_005267069.3:c.2816C>A	XP_005267126.2:p.Ala939Asp
XM_011535984.1:c.1766C>A	XP_011534286.1:p.Ala589Asp
XM_011535985.1:c.1586C>A	XP_011534287.1:p.Ala529Asp
XM_011535986.1:c.1346C>A	XP_011534288.1:p.Ala449Asp
XM_011535987.1:c.965C>A	XP_011534289.1:p.Ala322Asp
XM_011535988.1:c.-20+15720C>A	XP_011534290.1:n.-20+15720C>A
NM_001346813.1:c.2816C>A	NP_001333742.1:p.Ala939Asp
NM_001363725.1:c.566C>A	NP_001350654.1:p.Ala189Asp
XM_011535984.2:c.2897C>A	XP_011534286.2:p.Ala966Asp
XM_011535988.3:c.-20+15720C>A	XP_011534290.1:n.-20+15720C>A
XM_017011103.2:c.2897C>A	XP_016866592.1:p.Ala966Asp
XM_017011104.1:c.2897C>A	XP_016866593.1:p.Ala966Asp
XM_017011105.2:c.2897C>A	XP_016866594.1:p.Ala966Asp
XM_017011106.2:c.2897C>A	XP_016866595.1:p.Ala966Asp
XM_017011107.2:c.2717C>A	XP_016866596.1:p.Ala906Asp
XR_002956289.1:n.2980C>A
NM_001363725.2:c.566C>A	NP_001350654.1:p.Ala189Asp
NM_001371656.1:c.3104C>A	NP_001358585.1:p.Ala1035Asp
NM_001374820.1:c.3104C>A	NP_001361749.1:p.Ala1035Asp
NM_001374828.1:c.3065C>A MANE Select	NP_001361757.1:p.Ala1022Asp
NM_017519.3:c.3065C>A	NP_059989.3:p.Ala1022Asp