Canonical Allele Identifier: CA578797163
Gene: EN2 HGNC NCBI

Linked Data

gnomAD v2: 7-155254103-T-A
MyVariant Identifiers: chr7:g.155254103T>A (hg19) chr7:g.155461408T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461408T>A , CM000669.2:g.155461408T>A GRCh38
NC_000007.13:g.155254103T>A , CM000669.1:g.155254103T>A GRCh37
NC_000007.12:g.154946864T>A NCBI36
NG_007124.1:g.9689T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-963T>A MANE Select ENSP00000297375.4:n.686-963T>A
NM_001427.3:c.686-963T>A NP_001418.2:n.686-963T>A
NM_001427.4:c.686-963T>A MANE Select NP_001418.2:n.686-963T>A
Search 100 bp 5'
Search 100 bp 3'