Canonical Allele Identifier: CA1610840992
Gene: EDN1 HGNC NCBI

Linked Data

dbSNP Id: rs1762637012

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12290283C>T , CM000668.2:g.12290283C>T GRCh38
NC_000006.11:g.12290516C>T , CM000668.1:g.12290516C>T GRCh37
NC_000006.10:g.12398502C>T NCBI36
NG_016196.1:g.4988C>T

Transcript Alleles

HGVS Amino-acid Change
XM_011514330.1:c.-1-346C>T XP_011512632.1:n.-1-346C>T
XM_011514331.1:c.-1-346C>T XP_011512633.1:n.-1-346C>T
XM_011514332.1:c.-1-346C>T XP_011512634.1:n.-1-346C>T
XM_011514330.2:c.-1-346C>T XP_011512632.1:n.-1-346C>T
XM_011514331.3:c.-1-346C>T XP_011512633.1:n.-1-346C>T
XM_011514332.2:c.-1-346C>T XP_011512634.1:n.-1-346C>T
XM_017010331.1:c.-2+160C>T XP_016865820.1:n.-2+160C>T