Canonical Allele Identifier: CA448427971
Gene: EDN1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.12296261C>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12296028C>A , CM000668.2:g.12296028C>A GRCh38
NC_000006.11:g.12296261C>A , CM000668.1:g.12296261C>A GRCh37
NC_000006.10:g.12404247C>A NCBI36
NG_016196.1:g.10733C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379375.6:c.600C>A MANE Select ENSP00000368683.5:p.Ser200=
ENST00000379375.5:c.600C>A ENSP00000368683.5:p.Ser200=
NM_001168319.1:c.597C>A NP_001161791.1:p.Ser199=
NM_001955.4:c.600C>A NP_001946.3:p.Ser200=
XM_011514330.1:c.600C>A XP_011512632.1:p.Ser200=
XM_011514331.1:c.600C>A XP_011512633.1:p.Ser200=
XM_011514332.1:c.597C>A XP_011512634.1:p.Ser199=
XM_011514330.2:c.600C>A XP_011512632.1:p.Ser200=
XM_011514331.3:c.600C>A XP_011512633.1:p.Ser200=
XM_011514332.2:c.597C>A XP_011512634.1:p.Ser199=
XM_017010331.1:c.600C>A XP_016865820.1:p.Ser200=
NM_001955.5:c.600C>A MANE Select NP_001946.3:p.Ser200=
NM_001168319.2:c.597C>A NP_001161791.1:p.Ser199=