Canonical Allele Identifier: CA2128589102
Gene: EGLN3 HGNC NCBI

Linked Data

dbSNP Id: rs1882322161
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.34375113T>C , CM000676.2:g.34375113T>C GRCh38
NC_000014.8:g.34844319T>C , CM000676.1:g.34844319T>C GRCh37
NC_000014.7:g.33914070T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000551935.5:n.59+87603A>G
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