Canonical Allele Identifier: CA662056127
Gene: ADARB2 HGNC NCBI

Linked Data

dbSNP Id: rs1452345065
gnomAD v3: 10-1410636-C-G
gnomAD v4: 10-1410636-C-G
MyVariant Identifiers: chr10:g.1452831C>G (hg19) chr10:g.1410636C>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.1410636C>G , CM000672.2:g.1410636C>G GRCh38
NC_000010.10:g.1452831C>G , CM000672.1:g.1452831C>G GRCh37
NC_000010.9:g.1442831C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381312.6:c.101-31476G>C MANE Select ENSP00000370713.1:n.101-31476G>C
ENST00000381312.5:c.101-31476G>C ENSP00000370713.1:n.101-31476G>C
NM_018702.3:c.101-31476G>C NP_061172.1:n.101-31476G>C
XR_930468.1:n.449-31476G>C
NM_018702.4:c.101-31476G>C MANE Select NP_061172.1:n.101-31476G>C
Search 100 bp 5'
Search 100 bp 3'