Canonical Allele Identifier: CA662056138
Gene: ADARB2 HGNC NCBI

Linked Data

dbSNP Id: rs1259197406
gnomAD v3: 10-1410650-G-T
gnomAD v4: 10-1410650-G-T
MyVariant Identifiers: chr10:g.1452845G>T (hg19) chr10:g.1410650G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.1410650G>T , CM000672.2:g.1410650G>T GRCh38
NC_000010.10:g.1452845G>T , CM000672.1:g.1452845G>T GRCh37
NC_000010.9:g.1442845G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381312.6:c.101-31490C>A MANE Select ENSP00000370713.1:n.101-31490C>A
ENST00000381312.5:c.101-31490C>A ENSP00000370713.1:n.101-31490C>A
NM_018702.3:c.101-31490C>A NP_061172.1:n.101-31490C>A
XR_930468.1:n.449-31490C>A
NM_018702.4:c.101-31490C>A MANE Select NP_061172.1:n.101-31490C>A
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