Canonical Allele Identifier: CA2685784390
Gene: EN2 HGNC NCBI

Linked Data

gnomAD v4: 7-155463314-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155463314T>G , CM000669.2:g.155463314T>G GRCh38
NC_000007.13:g.155256009T>G , CM000669.1:g.155256009T>G GRCh37
NC_000007.12:g.154948770T>G NCBI36
NG_007124.1:g.11595T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.*627T>G MANE Select ENSP00000297375.4:n.*627T>G
NM_001427.3:c.*627T>G NP_001418.2:n.*627T>G
NM_001427.4:c.*627T>G MANE Select NP_001418.2:n.*627T>G
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