Canonical Allele Identifier: CA169339887
Gene: EN2 HGNC NCBI

Linked Data

dbSNP Id: rs190624074
gnomAD v2: 7-155253846-G-A
gnomAD v3: 7-155461151-G-A
gnomAD v4: 7-155461151-G-A
MyVariant Identifiers: chr7:g.155253846G>A (hg19) chr7:g.155461151G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.155461151G>A , CM000669.2:g.155461151G>A GRCh38
NC_000007.13:g.155253846G>A , CM000669.1:g.155253846G>A GRCh37
NC_000007.12:g.154946607G>A NCBI36
NG_007124.1:g.9432G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000297375.4:c.686-1220G>A MANE Select ENSP00000297375.4:n.686-1220G>A
NM_001427.3:c.686-1220G>A NP_001418.2:n.686-1220G>A
NM_001427.4:c.686-1220G>A MANE Select NP_001418.2:n.686-1220G>A
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