Canonical Allele Identifier: CA1610839230
Gene: EDN1 HGNC NCBI

Linked Data

dbSNP Id: rs1762610259

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12288922T>C , CM000668.2:g.12288922T>C GRCh38
NC_000006.11:g.12289155T>C , CM000668.1:g.12289155T>C GRCh37
NC_000006.10:g.12397141T>C NCBI36
NG_016196.1:g.3627T>C

Transcript Alleles

HGVS Amino-acid Change
XM_011514330.1:c.-2+427T>C XP_011512632.1:n.-2+427T>C
XM_011514331.1:c.-1-1707T>C XP_011512633.1:n.-1-1707T>C
XM_011514332.1:c.-2+427T>C XP_011512634.1:n.-2+427T>C
XM_011514330.2:c.-2+427T>C XP_011512632.1:n.-2+427T>C
XM_011514331.3:c.-1-1707T>C XP_011512633.1:n.-1-1707T>C
XM_011514332.2:c.-2+427T>C XP_011512634.1:n.-2+427T>C