Canonical Allele Identifier: CA134216865

Gene: EDN1

Linked Data

• dbSNP Id: rs938033541
• gnomAD v3: 6-12290300-C-T
• gnomAD v4: 6-12290300-C-T
• MyVariant Identifiers: chr6:g.12290533C>T (hg19) ; chr6:g.12290300C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12290300C>T , CM000668.2:g.12290300C>T	GRCh38
NC_000006.11:g.12290533C>T , CM000668.1:g.12290533C>T	GRCh37
NC_000006.10:g.12398519C>T	NCBI36
NG_016196.1:g.5005C>T

Transcript Alleles

HGVS	Amino-acid change
NM_001168319.1:c.-330C>T	NP_001161791.1:n.-330C>T
NM_001955.4:c.-330C>T	NP_001946.3:n.-330C>T
XM_011514330.1:c.-1-329C>T	XP_011512632.1:n.-1-329C>T
XM_011514331.1:c.-1-329C>T	XP_011512633.1:n.-1-329C>T
XM_011514332.1:c.-1-329C>T	XP_011512634.1:n.-1-329C>T
XM_011514330.2:c.-1-329C>T	XP_011512632.1:n.-1-329C>T
XM_011514331.3:c.-1-329C>T	XP_011512633.1:n.-1-329C>T
XM_011514332.2:c.-1-329C>T	XP_011512634.1:n.-1-329C>T
XM_017010331.1:c.-2+177C>T	XP_016865820.1:n.-2+177C>T