Canonical Allele Identifier: CA590983533
Gene: ADARB2 HGNC NCBI

Linked Data

gnomAD v2: 10-1452857-T-G
MyVariant Identifiers: chr10:g.1452857T>G (hg19) chr10:g.1410662T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.1410662T>G , CM000672.2:g.1410662T>G GRCh38
NC_000010.10:g.1452857T>G , CM000672.1:g.1452857T>G GRCh37
NC_000010.9:g.1442857T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000381312.6:c.101-31502A>C MANE Select ENSP00000370713.1:n.101-31502A>C
ENST00000381312.5:c.101-31502A>C ENSP00000370713.1:n.101-31502A>C
NM_018702.3:c.101-31502A>C NP_061172.1:n.101-31502A>C
XR_930468.1:n.449-31502A>C
NM_018702.4:c.101-31502A>C MANE Select NP_061172.1:n.101-31502A>C
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