Canonical Allele Identifier: CA662056178
Gene: ADARB2 HGNC NCBI

Linked Data

dbSNP Id: rs1214369663
gnomAD v3: 10-1410757-G-C
gnomAD v4: 10-1410757-G-C
MyVariant Identifiers: chr10:g.1452952G>C (hg19) chr10:g.1410757G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.1410757G>C , CM000672.2:g.1410757G>C GRCh38
NC_000010.10:g.1452952G>C , CM000672.1:g.1452952G>C GRCh37
NC_000010.9:g.1442952G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381312.6:c.101-31597C>G MANE Select ENSP00000370713.1:n.101-31597C>G
ENST00000381312.5:c.101-31597C>G ENSP00000370713.1:n.101-31597C>G
NM_018702.3:c.101-31597C>G NP_061172.1:n.101-31597C>G
XR_930468.1:n.449-31597C>G
NM_018702.4:c.101-31597C>G MANE Select NP_061172.1:n.101-31597C>G
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