Canonical Allele Identifier: CA1164818597

Gene: EDN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.41479041G= , CM000663.2:g.41479041G=	GRCh38
NC_000001.10:g.41944712G= , CM000663.1:g.41944712G=	GRCh37
NC_000001.9:g.41717299G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000372587.5:c.*368C= MANE Select	ENSP00000361668.4:n.*368C=
ENST00000372587.4:c.*368C=	ENSP00000361668.4:n.*368C=
NM_001302269.1:c.*368C=	NP_001289198.1:n.*368C=
NM_001956.4:c.*368C=	NP_001947.1:n.*368C=
NR_126098.1:n.896C=
XM_017000512.1:c.*368C=	XP_016856001.1:n.*368C=
NM_001956.5:c.*368C= MANE Select	NP_001947.1:n.*368C=
NM_001302269.2:c.*368C=	NP_001289198.1:n.*368C=
NR_126098.2:n.896C=