Canonical Allele Identifier: CA835693233
Gene: EN2 HGNC NCBI

Linked Data

dbSNP Id: rs1452218277
MyVariant Identifiers: chr7:g.155253698G>T (hg19) chr7:g.155461003G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461003G>T , CM000669.2:g.155461003G>T GRCh38
NC_000007.13:g.155253698G>T , CM000669.1:g.155253698G>T GRCh37
NC_000007.12:g.154946459G>T NCBI36
NG_007124.1:g.9284G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000297375.4:c.686-1368G>T MANE Select ENSP00000297375.4:n.686-1368G>T
NM_001427.3:c.686-1368G>T NP_001418.2:n.686-1368G>T
NM_001427.4:c.686-1368G>T MANE Select NP_001418.2:n.686-1368G>T
Search 100 bp 5'
Search 100 bp 3'