Canonical Allele Identifier: CA1754594940
Gene: EN2 HGNC NCBI

Linked Data

dbSNP Id: rs1795719638
gnomAD v4: 7-155463327-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155463327C>T , CM000669.2:g.155463327C>T GRCh38
NC_000007.13:g.155256022C>T , CM000669.1:g.155256022C>T GRCh37
NC_000007.12:g.154948783C>T NCBI36
NG_007124.1:g.11608C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.*640C>T MANE Select ENSP00000297375.4:n.*640C>T
NM_001427.3:c.*640C>T NP_001418.2:n.*640C>T
NM_001427.4:c.*640C>T MANE Select NP_001418.2:n.*640C>T
Search 100 bp 5'
Search 100 bp 3'