Canonical Allele Identifier: CA3638626
Gene: EDN1 HGNC NCBI

Linked Data

dbSNP Id: rs778827439
gnomAD v2: 6-12292619-A-G
gnomAD v3: 6-12292386-A-G
gnomAD v4: 6-12292386-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.12292386A>G , CM000668.2:g.12292386A>G GRCh38
NC_000006.11:g.12292619A>G , CM000668.1:g.12292619A>G GRCh37
NC_000006.10:g.12400605A>G NCBI36
NG_016196.1:g.7091A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379375.6:c.110A>G MANE Select ENSP00000368683.5:p.Glu37Gly
ENST00000379375.5:c.110A>G ENSP00000368683.5:p.Glu37Gly
NM_001168319.1:c.107A>G NP_001161791.1:p.Glu36Gly
NM_001955.4:c.110A>G NP_001946.3:p.Glu37Gly
XM_011514330.1:c.110A>G XP_011512632.1:p.Glu37Gly
XM_011514331.1:c.110A>G XP_011512633.1:p.Glu37Gly
XM_011514332.1:c.107A>G XP_011512634.1:p.Glu36Gly
XM_011514330.2:c.110A>G XP_011512632.1:p.Glu37Gly
XM_011514331.3:c.110A>G XP_011512633.1:p.Glu37Gly
XM_011514332.2:c.107A>G XP_011512634.1:p.Glu36Gly
XM_017010331.1:c.110A>G XP_016865820.1:p.Glu37Gly
NM_001955.5:c.110A>G MANE Select NP_001946.3:p.Glu37Gly
NM_001168319.2:c.107A>G NP_001161791.1:p.Glu36Gly