Canonical Allele Identifier: CA2128589109
Gene: EGLN3 HGNC NCBI

Linked Data

dbSNP Id: rs1882322303
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.34375128A>G , CM000676.2:g.34375128A>G GRCh38
NC_000014.8:g.34844334A>G , CM000676.1:g.34844334A>G GRCh37
NC_000014.7:g.33914085A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000551935.5:n.59+87588T>C
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