Canonical Allele Identifier: CA1825151

Linked Data

dbSNP Id: rs771332801

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108929341G>A , CM000664.2:g.108929341G>A GRCh38
NC_000002.11:g.109545797G>A , CM000664.1:g.109545797G>A GRCh37
NC_000002.10:g.108912229G>A NCBI36
NG_008257.1:g.65032C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000258443.7:c.213C>T (EDAR) MANE Select ENSP00000258443.2:p.Cys71=
ENST00000258443.6:c.213C>T (EDAR) ENSP00000258443.2:p.Cys71=
ENST00000376651.1:c.213C>T (EDAR) ENSP00000365839.1:p.Cys71=
ENST00000409271.5:c.213C>T (EDAR) ENSP00000386371.1:p.Cys71=
NM_022336.3:c.213C>T (EDAR) NP_071731.1:p.Cys71=
XM_006712204.1:c.213C>T (EDAR) XP_006712267.1:p.Cys71=
XM_011510502.1:c.264C>T (EDAR) XP_011508804.1:p.Cys88=
XM_011510503.1:c.264C>T (EDAR) XP_011508805.1:p.Cys88=
XM_011510502.2:c.357C>T (EDAR) XP_011508804.2:p.Cys119=
XM_011510503.2:c.357C>T (EDAR) XP_011508805.2:p.Cys119=
XM_017004623.2:c.8370+156295G>A (RANBP2) XP_016860112.1:n.8370+156295G>A
NM_022336.4:c.213C>T (EDAR) MANE Select NP_071731.1:p.Cys71=