Canonical Allele Identifier: CA1164818590
Gene: EDN2 HGNC NCBI

Linked Data

dbSNP Id: rs1644223220
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.41479030G>A , CM000663.2:g.41479030G>A GRCh38
NC_000001.10:g.41944701G>A , CM000663.1:g.41944701G>A GRCh37
NC_000001.9:g.41717288G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000372587.5:c.*379C>T MANE Select ENSP00000361668.4:n.*379C>T
ENST00000372587.4:c.*379C>T ENSP00000361668.4:n.*379C>T
NM_001302269.1:c.*379C>T NP_001289198.1:n.*379C>T
NM_001956.4:c.*379C>T NP_001947.1:n.*379C>T
NR_126098.1:n.907C>T
XM_017000512.1:c.*379C>T XP_016856001.1:n.*379C>T
NM_001956.5:c.*379C>T MANE Select NP_001947.1:n.*379C>T
NM_001302269.2:c.*379C>T NP_001289198.1:n.*379C>T
NR_126098.2:n.907C>T
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