Canonical Allele Identifier: CA590983523

Gene: ADARB2

Linked Data

• dbSNP Id: rs1261852532
• gnomAD v2: 10-1452594-A-G
• gnomAD v3: 10-1410399-A-G
• gnomAD v4: 10-1410399-A-G
• MyVariant Identifiers: chr10:g.1452594A>G (hg19) ; chr10:g.1410399A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.1410399A>G , CM000672.2:g.1410399A>G	GRCh38
NC_000010.10:g.1452594A>G , CM000672.1:g.1452594A>G	GRCh37
NC_000010.9:g.1442594A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000381312.6:c.101-31239T>C MANE Select	ENSP00000370713.1:n.101-31239T>C
ENST00000381312.5:c.101-31239T>C	ENSP00000370713.1:n.101-31239T>C
NM_018702.3:c.101-31239T>C	NP_061172.1:n.101-31239T>C
XR_930468.1:n.449-31239T>C
NM_018702.4:c.101-31239T>C MANE Select	NP_061172.1:n.101-31239T>C