Canonical Allele Identifier: CA1754593913
Gene: EN2 HGNC NCBI

Linked Data

dbSNP Id: rs1795690038
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461136C>A , CM000669.2:g.155461136C>A GRCh38
NC_000007.13:g.155253831C>A , CM000669.1:g.155253831C>A GRCh37
NC_000007.12:g.154946592C>A NCBI36
NG_007124.1:g.9417C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-1235C>A MANE Select ENSP00000297375.4:n.686-1235C>A
NM_001427.3:c.686-1235C>A NP_001418.2:n.686-1235C>A
NM_001427.4:c.686-1235C>A MANE Select NP_001418.2:n.686-1235C>A
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