Canonical Allele Identifier: CA662056118
Gene: ADARB2 HGNC NCBI

Linked Data

dbSNP Id: rs1383059803
gnomAD v3: 10-1410612-T-C
gnomAD v4: 10-1410612-T-C
MyVariant Identifiers: chr10:g.1452807T>C (hg19) chr10:g.1410612T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.1410612T>C , CM000672.2:g.1410612T>C GRCh38
NC_000010.10:g.1452807T>C , CM000672.1:g.1452807T>C GRCh37
NC_000010.9:g.1442807T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000381312.6:c.101-31452A>G MANE Select ENSP00000370713.1:n.101-31452A>G
ENST00000381312.5:c.101-31452A>G ENSP00000370713.1:n.101-31452A>G
NM_018702.3:c.101-31452A>G NP_061172.1:n.101-31452A>G
XR_930468.1:n.449-31452A>G
NM_018702.4:c.101-31452A>G MANE Select NP_061172.1:n.101-31452A>G
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