Canonical Allele Identifier: CA169340038
Gene: EN2 HGNC NCBI

Linked Data

dbSNP Id: rs566966015

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461269C>G , CM000669.2:g.155461269C>G GRCh38
NC_000007.13:g.155253964C>G , CM000669.1:g.155253964C>G GRCh37
NC_000007.12:g.154946725C>G NCBI36
NG_007124.1:g.9550C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-1102C>G MANE Select ENSP00000297375.4:n.686-1102C>G
NM_001427.3:c.686-1102C>G NP_001418.2:n.686-1102C>G
NM_001427.4:c.686-1102C>G MANE Select NP_001418.2:n.686-1102C>G