Canonical Allele Identifier: CA2729386097

Gene: EGLN3

Linked Data

• dbSNP Id: rs2138770706

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.34375124A>G , CM000676.2:g.34375124A>G	GRCh38
NC_000014.8:g.34844330A>G , CM000676.1:g.34844330A>G	GRCh37
NC_000014.7:g.33914081A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000551935.5:n.59+87592T>C