Canonical Allele Identifier: CA2128589097
Gene: EGLN3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.34375109T= , CM000676.2:g.34375109T= GRCh38
NC_000014.8:g.34844315T= , CM000676.1:g.34844315T= GRCh37
NC_000014.7:g.33914066T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000551935.5:n.59+87607A=