Canonical Allele Identifier: CA12623071

Gene: EN2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.155459499G>T , CM000669.2:g.155459499G>T	GRCh38
NC_000007.13:g.155252194G>T , CM000669.1:g.155252194G>T	GRCh37
NC_000007.12:g.154944955G>T	NCBI36
NG_007124.1:g.7780G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297375.4:c.685+437G>T MANE Select	ENSP00000297375.4:n.685+437G>T
NM_001427.3:c.685+437G>T	NP_001418.2:n.685+437G>T
NM_001427.4:c.685+437G>T MANE Select	NP_001418.2:n.685+437G>T