Canonical Allele Identifier: CA1086089656
Gene: EDN1 HGNC NCBI

Linked Data

dbSNP Id: rs1762637583
gnomAD v3: 6-12290307-C-T
gnomAD v4: 6-12290307-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12290307C>T , CM000668.2:g.12290307C>T GRCh38
NC_000006.11:g.12290540C>T , CM000668.1:g.12290540C>T GRCh37
NC_000006.10:g.12398526C>T NCBI36
NG_016196.1:g.5012C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001168319.1:c.-323C>T NP_001161791.1:n.-323C>T
NM_001955.4:c.-323C>T NP_001946.3:n.-323C>T
XM_011514330.1:c.-1-322C>T XP_011512632.1:n.-1-322C>T
XM_011514331.1:c.-1-322C>T XP_011512633.1:n.-1-322C>T
XM_011514332.1:c.-1-322C>T XP_011512634.1:n.-1-322C>T
XM_011514330.2:c.-1-322C>T XP_011512632.1:n.-1-322C>T
XM_011514331.3:c.-1-322C>T XP_011512633.1:n.-1-322C>T
XM_011514332.2:c.-1-322C>T XP_011512634.1:n.-1-322C>T
XM_017010331.1:c.-2+184C>T XP_016865820.1:n.-2+184C>T