Canonical Allele Identifier: CA961832518
Gene: EGLN3 HGNC NCBI

Linked Data

dbSNP Id: rs1882321455

Genomic Alleles

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

Transcript Alleles

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