Canonical Allele Identifier: CA1164818588
Gene: EDN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.41479027G= , CM000663.2:g.41479027G= GRCh38
NC_000001.10:g.41944698G= , CM000663.1:g.41944698G= GRCh37
NC_000001.9:g.41717285G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000372587.5:c.*382C= MANE Select ENSP00000361668.4:n.*382C=
ENST00000372587.4:c.*382C= ENSP00000361668.4:n.*382C=
NM_001302269.1:c.*382C= NP_001289198.1:n.*382C=
NM_001956.4:c.*382C= NP_001947.1:n.*382C=
NR_126098.1:n.910C=
XM_017000512.1:c.*382C= XP_016856001.1:n.*382C=
NM_001956.5:c.*382C= MANE Select NP_001947.1:n.*382C=
NM_001302269.2:c.*382C= NP_001289198.1:n.*382C=
NR_126098.2:n.910C=
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