Canonical Allele Identifier: CA362857342

Gene: EDN1

Linked Data

• gnomAD v4: 6-12296018-G-T
• MyVariant Identifiers: chr6:g.12296251G>T (hg19) ; chr6:g.12296018G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12296018G>T , CM000668.2:g.12296018G>T	GRCh38
NC_000006.11:g.12296251G>T , CM000668.1:g.12296251G>T	GRCh37
NC_000006.10:g.12404237G>T	NCBI36
NG_016196.1:g.10723G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.590G>T MANE Select	ENSP00000368683.5:p.Gly197Val
ENST00000379375.5:c.590G>T	ENSP00000368683.5:p.Gly197Val
NM_001168319.1:c.587G>T	NP_001161791.1:p.Gly196Val
NM_001955.4:c.590G>T	NP_001946.3:p.Gly197Val
XM_011514330.1:c.590G>T	XP_011512632.1:p.Gly197Val
XM_011514331.1:c.590G>T	XP_011512633.1:p.Gly197Val
XM_011514332.1:c.587G>T	XP_011512634.1:p.Gly196Val
XM_011514330.2:c.590G>T	XP_011512632.1:p.Gly197Val
XM_011514331.3:c.590G>T	XP_011512633.1:p.Gly197Val
XM_011514332.2:c.587G>T	XP_011512634.1:p.Gly196Val
XM_017010331.1:c.590G>T	XP_016865820.1:p.Gly197Val
NM_001955.5:c.590G>T MANE Select	NP_001946.3:p.Gly197Val
NM_001168319.2:c.587G>T	NP_001161791.1:p.Gly196Val