Canonical Allele Identifier: CA362856960

Gene: EDN1

Linked Data

• dbSNP Id: rs1762767268
• gnomAD v3: 6-12294296-A-G
• gnomAD v4: 6-12294296-A-G
• MyVariant Identifiers: chr6:g.12294529A>G (hg19) ; chr6:g.12294296A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12294296A>G , CM000668.2:g.12294296A>G	GRCh38
NC_000006.11:g.12294529A>G , CM000668.1:g.12294529A>G	GRCh37
NC_000006.10:g.12402515A>G	NCBI36
NG_016196.1:g.9001A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.425A>G MANE Select	ENSP00000368683.5:p.His142Arg
ENST00000379375.5:c.425A>G	ENSP00000368683.5:p.His142Arg
NM_001168319.1:c.422A>G	NP_001161791.1:p.His141Arg
NM_001955.4:c.425A>G	NP_001946.3:p.His142Arg
XM_011514330.1:c.425A>G	XP_011512632.1:p.His142Arg
XM_011514331.1:c.425A>G	XP_011512633.1:p.His142Arg
XM_011514332.1:c.422A>G	XP_011512634.1:p.His141Arg
XM_011514330.2:c.425A>G	XP_011512632.1:p.His142Arg
XM_011514331.3:c.425A>G	XP_011512633.1:p.His142Arg
XM_011514332.2:c.422A>G	XP_011512634.1:p.His141Arg
XM_017010331.1:c.425A>G	XP_016865820.1:p.His142Arg
NM_001955.5:c.425A>G MANE Select	NP_001946.3:p.His142Arg
NM_001168319.2:c.422A>G	NP_001161791.1:p.His141Arg