Canonical Allele Identifier: CA366382830

Gene: ARID1B

Linked Data

• gnomAD v4: 6-156778702-A-C
• MyVariant Identifiers: chr6:g.157099836A>C (hg19) ; chr6:g.156778702A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.156778702A>C , CM000668.2:g.156778702A>C	GRCh38
NC_000006.11:g.157099836A>C , CM000668.1:g.157099836A>C	GRCh37
NC_000006.10:g.157141528A>C	NCBI36
NG_032093.1:g.5773A>C
NG_032093.2:g.5773A>C
NG_066624.1:g.7677A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000350026.11:c.1022A>C	ENSP00000055163.8:p.Gln341Pro
ENST00000414678.8:c.1022A>C	ENSP00000412835.3:p.Gln341Pro
ENST00000637015.2:c.1022A>C	ENSP00000489729.2:p.Gln341Pro
ENST00000346085.10:c.1022A>C	ENSP00000344546.5:p.Gln341Pro
ENST00000350026.10:c.773A>C	ENSP00000055163.7:p.Gln258Pro
ENST00000636930.2:c.1022A>C MANE Select	ENSP00000490491.2:p.Gln341Pro
ENST00000647938.1:c.773A>C	ENSP00000498155.1:p.Gln258Pro
ENST00000674298.1:c.762A>C
ENST00000346085.9:c.773A>C	ENSP00000344546.4:p.Gln258Pro
ENST00000350026.9:c.773A>C	ENSP00000055163.7:p.Gln258Pro
NM_017519.2:c.773A>C	NP_059989.2:p.Gln258Pro
NM_020732.3:c.773A>C	NP_065783.3:p.Gln258Pro
XM_005267069.3:c.773A>C	XP_005267126.2:p.Gln258Pro
NM_001346813.1:c.773A>C	NP_001333742.1:p.Gln258Pro
XM_011535984.2:c.773A>C	XP_011534286.2:p.Gln258Pro
XM_017011103.2:c.773A>C	XP_016866592.1:p.Gln258Pro
XM_017011104.1:c.773A>C	XP_016866593.1:p.Gln258Pro
XM_017011105.2:c.773A>C	XP_016866594.1:p.Gln258Pro
XM_017011106.2:c.773A>C	XP_016866595.1:p.Gln258Pro
XM_017011107.2:c.773A>C	XP_016866596.1:p.Gln258Pro
XR_002956289.1:n.856A>C
NM_001371656.1:c.1022A>C	NP_001358585.1:p.Gln341Pro
NM_001374820.1:c.1022A>C	NP_001361749.1:p.Gln341Pro
NM_001374828.1:c.1022A>C MANE Select	NP_001361757.1:p.Gln341Pro
NM_017519.3:c.1022A>C	NP_059989.3:p.Gln341Pro