Canonical Allele Identifier: CA521909910

Gene: ARID1A

Linked Data

• dbSNP Id: rs1274662499
• gnomAD v2: 1-27022864-G-C
• gnomAD v3: 1-26696373-G-C
• gnomAD v4: 1-26696373-G-C
• MyVariant Identifiers: chr1:g.27022864G>C (hg19) ; chr1:g.26696373G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696373G>C , CM000663.2:g.26696373G>C	GRCh38
NC_000001.10:g.27022864G>C , CM000663.1:g.27022864G>C	GRCh37
NC_000001.9:g.26895451G>C	NCBI36
NG_029965.1:g.5343G>C , LRG_875:g.5343G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.-31G>C MANE Select	ENSP00000320485.7:n.-31G>C
ENST00000430799.7:c.-13+2756G>C	ENSP00000390317.3:n.-13+2756G>C
ENST00000637465.1:c.-13+273G>C	ENSP00000490650.1:n.-13+273G>C
ENST00000324856.11:c.-31G>C	ENSP00000320485.7:n.-31G>C
NM_006015.4:c.-31G>C , LRG_875t1:c.-31G>C	NP_006006.3:n.-31G>C
NM_139135.2:c.-31G>C	NP_624361.1:n.-31G>C
XM_011542542.1:c.33C>G	XP_011540844.1:p.Pro11=
NM_006015.5:c.-31G>C	NP_006006.3:n.-31G>C
NM_139135.3:c.-31G>C	NP_624361.1:n.-31G>C
NM_006015.6:c.-31G>C MANE Select	NP_006006.3:n.-31G>C
NM_139135.4:c.-31G>C	NP_624361.1:n.-31G>C