Canonical Allele Identifier: CA169339927
Gene: EN2 HGNC NCBI

Linked Data

dbSNP Id: rs926737430
gnomAD v3: 7-155461160-C-T
gnomAD v4: 7-155461160-C-T
MyVariant Identifiers: chr7:g.155253855C>T (hg19) chr7:g.155461160C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461160C>T , CM000669.2:g.155461160C>T GRCh38
NC_000007.13:g.155253855C>T , CM000669.1:g.155253855C>T GRCh37
NC_000007.12:g.154946616C>T NCBI36
NG_007124.1:g.9441C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-1211C>T MANE Select ENSP00000297375.4:n.686-1211C>T
NM_001427.3:c.686-1211C>T NP_001418.2:n.686-1211C>T
NM_001427.4:c.686-1211C>T MANE Select NP_001418.2:n.686-1211C>T
Search 100 bp 5'
Search 100 bp 3'