Canonical Allele Identifier: CA2128589071
Gene: EGLN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.34375086T= , CM000676.2:g.34375086T= GRCh38
NC_000014.8:g.34844292T= , CM000676.1:g.34844292T= GRCh37
NC_000014.7:g.33914043T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000551935.5:n.59+87630A=