Canonical Allele Identifier: CA1164818586
Gene: EDN2 HGNC NCBI

Linked Data

dbSNP Id: rs1644223169
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.41479023C>T , CM000663.2:g.41479023C>T GRCh38
NC_000001.10:g.41944694C>T , CM000663.1:g.41944694C>T GRCh37
NC_000001.9:g.41717281C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000372587.5:c.*386G>A MANE Select ENSP00000361668.4:n.*386G>A
ENST00000372587.4:c.*386G>A ENSP00000361668.4:n.*386G>A
NM_001302269.1:c.*386G>A NP_001289198.1:n.*386G>A
NM_001956.4:c.*386G>A NP_001947.1:n.*386G>A
NR_126098.1:n.914G>A
XM_017000512.1:c.*386G>A XP_016856001.1:n.*386G>A
NM_001956.5:c.*386G>A MANE Select NP_001947.1:n.*386G>A
NM_001302269.2:c.*386G>A NP_001289198.1:n.*386G>A
NR_126098.2:n.914G>A
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