Canonical Allele Identifier: CA2187167423
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329605G= , CM000677.2:g.73329605G= GRCh38
NC_000015.9:g.73621946G= , CM000677.1:g.73621946G= GRCh37
NC_000015.8:g.71408999G= NCBI36
NG_009063.1:g.44660C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1558C= MANE Select ENSP00000261917.3:p.Leu520=
ENST00000261917.3:c.1558C= ENSP00000261917.3:p.Leu520=
NM_005477.2:c.1558C= NP_005468.1:p.Leu520=
XM_011521148.1:c.340C= XP_011519450.1:p.Leu114=
XM_011521148.2:c.340C= XP_011519450.1:p.Leu114=
NM_005477.3:c.1558C= MANE Select NP_005468.1:p.Leu520=