Canonical Allele Identifier: CA366381178

Gene: ARID1B

Linked Data

• dbSNP Id: rs1778769111
• gnomAD v4: 6-156778053-G-T
• MyVariant Identifiers: chr6:g.157099187G>T (hg19) ; chr6:g.156778053G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156778053G>T , CM000668.2:g.156778053G>T	GRCh38
NC_000006.11:g.157099187G>T , CM000668.1:g.157099187G>T	GRCh37
NC_000006.10:g.157140879G>T	NCBI36
NG_032093.1:g.5124G>T
NG_032093.2:g.5124G>T
NG_066624.1:g.7028G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.373G>T	ENSP00000055163.8:p.Ala125Ser
ENST00000414678.8:c.373G>T	ENSP00000412835.3:p.Ala125Ser
ENST00000637015.2:c.373G>T	ENSP00000489729.2:p.Ala125Ser
ENST00000346085.10:c.373G>T	ENSP00000344546.5:p.Ala125Ser
ENST00000350026.10:c.124G>T	ENSP00000055163.7:p.Ala42Ser
ENST00000636930.2:c.373G>T MANE Select	ENSP00000490491.2:p.Ala125Ser
ENST00000647938.1:c.124G>T	ENSP00000498155.1:p.Ala42Ser
ENST00000674298.1:c.113G>T
ENST00000346085.9:c.124G>T	ENSP00000344546.4:p.Ala42Ser
ENST00000350026.9:c.124G>T	ENSP00000055163.7:p.Ala42Ser
NM_017519.2:c.124G>T	NP_059989.2:p.Ala42Ser
NM_020732.3:c.124G>T	NP_065783.3:p.Ala42Ser
XM_005267069.3:c.124G>T	XP_005267126.2:p.Ala42Ser
XR_943148.1:n.177+193C>A
NM_001346813.1:c.124G>T	NP_001333742.1:p.Ala42Ser
XM_011535984.2:c.124G>T	XP_011534286.2:p.Ala42Ser
XM_017011103.2:c.124G>T	XP_016866592.1:p.Ala42Ser
XM_017011104.1:c.124G>T	XP_016866593.1:p.Ala42Ser
XM_017011105.2:c.124G>T	XP_016866594.1:p.Ala42Ser
XM_017011106.2:c.124G>T	XP_016866595.1:p.Ala42Ser
XM_017011107.2:c.124G>T	XP_016866596.1:p.Ala42Ser
XR_002956289.1:n.207G>T
NM_001371656.1:c.373G>T	NP_001358585.1:p.Ala125Ser
NM_001374820.1:c.373G>T	NP_001361749.1:p.Ala125Ser
NM_001374828.1:c.373G>T MANE Select	NP_001361757.1:p.Ala125Ser
NM_017519.3:c.373G>T	NP_059989.3:p.Ala125Ser
NR_163974.1:n.273+193C>A