Canonical Allele Identifier: CA2128589079
Gene: EGLN3 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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