Canonical Allele Identifier: CA2742062422
Gene: EDN2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.41479024A>G , CM000663.2:g.41479024A>G GRCh38
NC_000001.10:g.41944695A>G , CM000663.1:g.41944695A>G GRCh37
NC_000001.9:g.41717282A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000372587.5:c.*385T>C MANE Select ENSP00000361668.4:n.*385T>C
ENST00000372587.4:c.*385T>C ENSP00000361668.4:n.*385T>C
NM_001302269.1:c.*385T>C NP_001289198.1:n.*385T>C
NM_001956.4:c.*385T>C NP_001947.1:n.*385T>C
NR_126098.1:n.913T>C
XM_017000512.1:c.*385T>C XP_016856001.1:n.*385T>C
NM_001956.5:c.*385T>C MANE Select NP_001947.1:n.*385T>C
NM_001302269.2:c.*385T>C NP_001289198.1:n.*385T>C
NR_126098.2:n.913T>C
Search 100 bp 5'
Search 100 bp 3'