Canonical Allele Identifier: CA169340202
Gene: EN2 HGNC NCBI

Linked Data

dbSNP Id: rs772272907

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461348C>T , CM000669.2:g.155461348C>T GRCh38
NC_000007.13:g.155254043C>T , CM000669.1:g.155254043C>T GRCh37
NC_000007.12:g.154946804C>T NCBI36
NG_007124.1:g.9629C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-1023C>T MANE Select ENSP00000297375.4:n.686-1023C>T
NM_001427.3:c.686-1023C>T NP_001418.2:n.686-1023C>T
NM_001427.4:c.686-1023C>T MANE Select NP_001418.2:n.686-1023C>T