Canonical Allele Identifier: CA1610841059
Gene: EDN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12290331A= , CM000668.2:g.12290331A= GRCh38
NC_000006.11:g.12290564A= , CM000668.1:g.12290564A= GRCh37
NC_000006.10:g.12398550A= NCBI36
NG_016196.1:g.5036A=

Transcript Alleles

HGVS Amino-acid Change
NM_001168319.1:c.-299A= NP_001161791.1:n.-299A=
NM_001955.4:c.-299A= NP_001946.3:n.-299A=
XM_011514330.1:c.-1-298A= XP_011512632.1:n.-1-298A=
XM_011514331.1:c.-1-298A= XP_011512633.1:n.-1-298A=
XM_011514332.1:c.-1-298A= XP_011512634.1:n.-1-298A=
XM_011514330.2:c.-1-298A= XP_011512632.1:n.-1-298A=
XM_011514331.3:c.-1-298A= XP_011512633.1:n.-1-298A=
XM_011514332.2:c.-1-298A= XP_011512634.1:n.-1-298A=
XM_017010331.1:c.-2+208A= XP_016865820.1:n.-2+208A=