Canonical Allele Identifier: CA2128589062
Gene: EGLN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.34375075A= , CM000676.2:g.34375075A= GRCh38
NC_000014.8:g.34844281A= , CM000676.1:g.34844281A= GRCh37
NC_000014.7:g.33914032A= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000551935.5:n.59+87641T=