Canonical Allele Identifier: CA3638768

Gene: EDN1

Linked Data

• dbSNP Id: rs775517180
• ExAC: 6:12296240 C / T
• gnomAD v2: 6-12296240-C-T
• gnomAD v4: 6-12296007-C-T
• MyVariant Identifiers: chr6:g.12296240C>T (hg19) ; chr6:g.12296007C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.12296007C>T , CM000668.2:g.12296007C>T	GRCh38
NC_000006.11:g.12296240C>T , CM000668.1:g.12296240C>T	GRCh37
NC_000006.10:g.12404226C>T	NCBI36
NG_016196.1:g.10712C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379375.6:c.579C>T MANE Select	ENSP00000368683.5:p.Pro193=
ENST00000379375.5:c.579C>T	ENSP00000368683.5:p.Pro193=
NM_001168319.1:c.576C>T	NP_001161791.1:p.Pro192=
NM_001955.4:c.579C>T	NP_001946.3:p.Pro193=
XM_011514330.1:c.579C>T	XP_011512632.1:p.Pro193=
XM_011514331.1:c.579C>T	XP_011512633.1:p.Pro193=
XM_011514332.1:c.576C>T	XP_011512634.1:p.Pro192=
XM_011514330.2:c.579C>T	XP_011512632.1:p.Pro193=
XM_011514331.3:c.579C>T	XP_011512633.1:p.Pro193=
XM_011514332.2:c.576C>T	XP_011512634.1:p.Pro192=
XM_017010331.1:c.579C>T	XP_016865820.1:p.Pro193=
NM_001955.5:c.579C>T MANE Select	NP_001946.3:p.Pro193=
NM_001168319.2:c.576C>T	NP_001161791.1:p.Pro192=