Canonical Allele Identifier: CA66116933
Gene: DIRC3 HGNC NCBI

Linked Data

dbSNP Id: rs1056954885
MyVariant Identifiers: chr2:g.218310441A>G (hg19) chr2:g.217445718A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.217445718A>G , CM000664.2:g.217445718A>G GRCh38
NC_000002.11:g.218310441A>G , CM000664.1:g.218310441A>G GRCh37
NC_000002.10:g.218018686A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000474063.5:n.500-11602T>C
ENST00000486365.5:n.1523-11602T>C
NR_026597.1:n.1523-11602T>C
NR_026597.2:n.1523-11602T>C
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