Canonical Allele Identifier: CA339264249

Gene: ARID1A

Linked Data

• dbSNP Id: rs1342376116
• gnomAD v4: 1-26696438-G-C
• MyVariant Identifiers: chr1:g.27022929G>C (hg19) ; chr1:g.26696438G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.26696438G>C , CM000663.2:g.26696438G>C	GRCh38
NC_000001.10:g.27022929G>C , CM000663.1:g.27022929G>C	GRCh37
NC_000001.9:g.26895516G>C	NCBI36
NG_029965.1:g.5408G>C , LRG_875:g.5408G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324856.13:c.35G>C MANE Select	ENSP00000320485.7:p.Ser12Thr
ENST00000430799.7:c.-13+2821G>C	ENSP00000390317.3:n.-13+2821G>C
ENST00000637465.1:c.-13+338G>C	ENSP00000490650.1:n.-13+338G>C
ENST00000324856.11:c.35G>C	ENSP00000320485.7:p.Ser12Thr
ENST00000457599.6:c.35G>C	ENSP00000387636.2:p.Ser12Thr
NM_006015.4:c.35G>C , LRG_875t1:c.35G>C	NP_006006.3:p.Ser12Thr
NM_139135.2:c.35G>C	NP_624361.1:p.Ser12Thr
NM_006015.5:c.35G>C	NP_006006.3:p.Ser12Thr
NM_139135.3:c.35G>C	NP_624361.1:p.Ser12Thr
NM_006015.6:c.35G>C MANE Select	NP_006006.3:p.Ser12Thr
NM_139135.4:c.35G>C	NP_624361.1:p.Ser12Thr