Canonical Allele Identifier: CA259250701
Gene: EGLN3 HGNC NCBI

Linked Data

dbSNP Id: rs747324115
MyVariant Identifiers: chr14:g.34844280A>G (hg19) chr14:g.34375074A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.34375074A>G , CM000676.2:g.34375074A>G GRCh38
NC_000014.8:g.34844280A>G , CM000676.1:g.34844280A>G GRCh37
NC_000014.7:g.33914031A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000551935.5:n.59+87642T>C
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