Canonical Allele Identifier: CA2742062428
Gene: EDN2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.41479032C>G , CM000663.2:g.41479032C>G GRCh38
NC_000001.10:g.41944703C>G , CM000663.1:g.41944703C>G GRCh37
NC_000001.9:g.41717290C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000372587.5:c.*377G>C MANE Select ENSP00000361668.4:n.*377G>C
ENST00000372587.4:c.*377G>C ENSP00000361668.4:n.*377G>C
NM_001302269.1:c.*377G>C NP_001289198.1:n.*377G>C
NM_001956.4:c.*377G>C NP_001947.1:n.*377G>C
NR_126098.1:n.905G>C
XM_017000512.1:c.*377G>C XP_016856001.1:n.*377G>C
NM_001956.5:c.*377G>C MANE Select NP_001947.1:n.*377G>C
NM_001302269.2:c.*377G>C NP_001289198.1:n.*377G>C
NR_126098.2:n.905G>C
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