Canonical Allele Identifier: CA662056142
Gene: ADARB2 HGNC NCBI

Linked Data

dbSNP Id: rs1212462584
gnomAD v3: 10-1410658-T-G
gnomAD v4: 10-1410658-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.1410658T>G , CM000672.2:g.1410658T>G GRCh38
NC_000010.10:g.1452853T>G , CM000672.1:g.1452853T>G GRCh37
NC_000010.9:g.1442853T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381312.6:c.101-31498A>C MANE Select ENSP00000370713.1:n.101-31498A>C
ENST00000381312.5:c.101-31498A>C ENSP00000370713.1:n.101-31498A>C
NM_018702.3:c.101-31498A>C NP_061172.1:n.101-31498A>C
XR_930468.1:n.449-31498A>C
NM_018702.4:c.101-31498A>C MANE Select NP_061172.1:n.101-31498A>C