Canonical Allele Identifier: CA2711044270
Gene: EDN1 HGNC NCBI

Linked Data

dbSNP Id: rs2113790768

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12288912G>A , CM000668.2:g.12288912G>A GRCh38
NC_000006.11:g.12289145G>A , CM000668.1:g.12289145G>A GRCh37
NC_000006.10:g.12397131G>A NCBI36
NG_016196.1:g.3617G>A

Transcript Alleles

HGVS Amino-acid change
XM_011514330.1:c.-2+417G>A XP_011512632.1:n.-2+417G>A
XM_011514331.1:c.-1-1717G>A XP_011512633.1:n.-1-1717G>A
XM_011514332.1:c.-2+417G>A XP_011512634.1:n.-2+417G>A
XM_011514330.2:c.-2+417G>A XP_011512632.1:n.-2+417G>A
XM_011514331.3:c.-1-1717G>A XP_011512633.1:n.-1-1717G>A
XM_011514332.2:c.-2+417G>A XP_011512634.1:n.-2+417G>A