Canonical Allele Identifier: CA2128589080
Gene: EGLN3 HGNC NCBI

Linked Data

dbSNP Id: rs1882321675
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.34375091C>T , CM000676.2:g.34375091C>T GRCh38
NC_000014.8:g.34844297C>T , CM000676.1:g.34844297C>T GRCh37
NC_000014.7:g.33914048C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000551935.5:n.59+87625G>A
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