Canonical Allele Identifier: CA428204061

Linked Data

MyVariant Identifiers: chr2:g.109513510G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.108897054G>T , CM000664.2:g.108897054G>T GRCh38
NC_000002.11:g.109513510G>T , CM000664.1:g.109513510G>T GRCh37
NC_000002.10:g.108879942G>T NCBI36
NG_008257.1:g.97319C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000258443.7:c.1200C>A (EDAR) MANE Select ENSP00000258443.2:p.Arg400=
ENST00000258443.6:c.1200C>A (EDAR) ENSP00000258443.2:p.Arg400=
ENST00000376651.1:c.1296C>A (EDAR) ENSP00000365839.1:p.Arg432=
ENST00000409271.5:c.1296C>A (EDAR) ENSP00000386371.1:p.Arg432=
NM_022336.3:c.1200C>A (EDAR) NP_071731.1:p.Arg400=
XM_006712204.1:c.1296C>A (EDAR) XP_006712267.1:p.Arg432=
XM_011510502.1:c.1347C>A (EDAR) XP_011508804.1:p.Arg449=
XM_011510503.1:c.1251C>A (EDAR) XP_011508805.1:p.Arg417=
XM_011510504.1:c.627C>A (EDAR) XP_011508806.1:p.Arg209=
XM_011510502.2:c.1440C>A (EDAR) XP_011508804.2:p.Arg480=
XM_011510503.2:c.1344C>A (EDAR) XP_011508805.2:p.Arg448=
XM_017004623.2:c.8370+124008G>T (RANBP2) XP_016860112.1:n.8370+124008G>T
NM_022336.4:c.1200C>A (EDAR) MANE Select NP_071731.1:p.Arg400=