Canonical Allele Identifier: CA366389271

Gene: ARID1B

Linked Data

• dbSNP Id: rs1427793472
• gnomAD v2: 6-157470067-C-T
• gnomAD v3: 6-157148933-C-T
• gnomAD v4: 6-157148933-C-T
• MyVariant Identifiers: chr6:g.157470067C>T (hg19) ; chr6:g.157148933C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157148933C>T , CM000668.2:g.157148933C>T	GRCh38
NC_000006.11:g.157470067C>T , CM000668.1:g.157470067C>T	GRCh37
NC_000006.10:g.157511759C>T	NCBI36
NG_032093.1:g.376004C>T
NG_032093.2:g.376004C>T
NG_066624.1:g.377908C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.3071C>T	ENSP00000055163.8:p.Ala1024Val
ENST00000414678.8:c.2981C>T	ENSP00000412835.3:p.Ala994Val
ENST00000637015.2:c.3071C>T	ENSP00000489729.2:p.Ala1024Val
ENST00000319584.11:c.1085C>T	ENSP00000313006.7:p.Ala362Val
ENST00000346085.10:c.3110C>T	ENSP00000344546.5:p.Ala1037Val
ENST00000350026.10:c.2822C>T	ENSP00000055163.7:p.Ala941Val
ENST00000414678.7:c.1229C>T	ENSP00000412835.2:p.Ala410Val
ENST00000452544.2:n.972C>T
ENST00000635849.1:c.392C>T	ENSP00000490948.1:p.Ala131Val
ENST00000635957.1:c.26C>T	ENSP00000490385.1:p.Ala9Val
ENST00000636426.1:n.205C>T
ENST00000636930.2:c.3071C>T MANE Select	ENSP00000490491.2:p.Ala1024Val
ENST00000637015.1:c.310C>T
ENST00000637568.1:c.114C>T
ENST00000637810.1:c.572C>T	ENSP00000489636.1:p.Ala191Val
ENST00000637904.1:c.572C>T	ENSP00000490550.1:p.Ala191Val
ENST00000647938.1:c.2861C>T	ENSP00000498155.1:p.Ala954Val
ENST00000674190.1:n.1820C>T
ENST00000319584.10:c.1088C>T	ENSP00000313006.6:p.Ala363Val
ENST00000346085.9:c.2861C>T	ENSP00000344546.4:p.Ala954Val
ENST00000350026.9:c.2822C>T	ENSP00000055163.7:p.Ala941Val
ENST00000400790.3:c.23C>T	ENSP00000383596.3:p.Ala8Val
ENST00000414678.6:c.1229C>T	ENSP00000412835.2:p.Ala410Val
ENST00000452544.1:n.918C>T
ENST00000478761.3:c.144C>T
NM_017519.2:c.2822C>T	NP_059989.2:p.Ala941Val
NM_020732.3:c.2861C>T	NP_065783.3:p.Ala954Val
XM_005267069.3:c.2822C>T	XP_005267126.2:p.Ala941Val
XM_011535984.1:c.1772C>T	XP_011534286.1:p.Ala591Val
XM_011535985.1:c.1592C>T	XP_011534287.1:p.Ala531Val
XM_011535986.1:c.1352C>T	XP_011534288.1:p.Ala451Val
XM_011535987.1:c.971C>T	XP_011534289.1:p.Ala324Val
XM_011535988.1:c.-20+15726C>T	XP_011534290.1:n.-20+15726C>T
NM_001346813.1:c.2822C>T	NP_001333742.1:p.Ala941Val
NM_001363725.1:c.572C>T	NP_001350654.1:p.Ala191Val
XM_011535984.2:c.2903C>T	XP_011534286.2:p.Ala968Val
XM_011535988.3:c.-20+15726C>T	XP_011534290.1:n.-20+15726C>T
XM_017011103.2:c.2903C>T	XP_016866592.1:p.Ala968Val
XM_017011104.1:c.2903C>T	XP_016866593.1:p.Ala968Val
XM_017011105.2:c.2903C>T	XP_016866594.1:p.Ala968Val
XM_017011106.2:c.2903C>T	XP_016866595.1:p.Ala968Val
XM_017011107.2:c.2723C>T	XP_016866596.1:p.Ala908Val
XR_002956289.1:n.2986C>T
NM_001363725.2:c.572C>T	NP_001350654.1:p.Ala191Val
NM_001371656.1:c.3110C>T	NP_001358585.1:p.Ala1037Val
NM_001374820.1:c.3110C>T	NP_001361749.1:p.Ala1037Val
NM_001374828.1:c.3071C>T MANE Select	NP_001361757.1:p.Ala1024Val
NM_017519.3:c.3071C>T	NP_059989.3:p.Ala1024Val