Canonical Allele Identifier: CA1754594046
Gene: EN2 HGNC NCBI

Linked Data

dbSNP Id: rs1795693756
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461388G>T , CM000669.2:g.155461388G>T GRCh38
NC_000007.13:g.155254083G>T , CM000669.1:g.155254083G>T GRCh37
NC_000007.12:g.154946844G>T NCBI36
NG_007124.1:g.9669G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-983G>T MANE Select ENSP00000297375.4:n.686-983G>T
NM_001427.3:c.686-983G>T NP_001418.2:n.686-983G>T
NM_001427.4:c.686-983G>T MANE Select NP_001418.2:n.686-983G>T
Search 100 bp 5'
Search 100 bp 3'