Canonical Allele Identifier: CA3638773
Gene: EDN1 HGNC NCBI

Linked Data

dbSNP Id: rs750777751
gnomAD v2: 6-12296258-C-T
gnomAD v4: 6-12296025-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12296025C>T , CM000668.2:g.12296025C>T GRCh38
NC_000006.11:g.12296258C>T , CM000668.1:g.12296258C>T GRCh37
NC_000006.10:g.12404244C>T NCBI36
NG_016196.1:g.10730C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000379375.6:c.597C>T MANE Select ENSP00000368683.5:p.Pro199=
ENST00000379375.5:c.597C>T ENSP00000368683.5:p.Pro199=
NM_001168319.1:c.594C>T NP_001161791.1:p.Pro198=
NM_001955.4:c.597C>T NP_001946.3:p.Pro199=
XM_011514330.1:c.597C>T XP_011512632.1:p.Pro199=
XM_011514331.1:c.597C>T XP_011512633.1:p.Pro199=
XM_011514332.1:c.594C>T XP_011512634.1:p.Pro198=
XM_011514330.2:c.597C>T XP_011512632.1:p.Pro199=
XM_011514331.3:c.597C>T XP_011512633.1:p.Pro199=
XM_011514332.2:c.594C>T XP_011512634.1:p.Pro198=
XM_017010331.1:c.597C>T XP_016865820.1:p.Pro199=
NM_001955.5:c.597C>T MANE Select NP_001946.3:p.Pro199=
NM_001168319.2:c.594C>T NP_001161791.1:p.Pro198=