Canonical Allele Identifier: CA2685784405
Gene: EN2 HGNC NCBI

Linked Data

gnomAD v4: 7-155463329-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155463329A>T , CM000669.2:g.155463329A>T GRCh38
NC_000007.13:g.155256024A>T , CM000669.1:g.155256024A>T GRCh37
NC_000007.12:g.154948785A>T NCBI36
NG_007124.1:g.11610A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.*642A>T MANE Select ENSP00000297375.4:n.*642A>T
NM_001427.3:c.*642A>T NP_001418.2:n.*642A>T
NM_001427.4:c.*642A>T MANE Select NP_001418.2:n.*642A>T
Search 100 bp 5'
Search 100 bp 3'