Canonical Allele Identifier: CA2187169774
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332178G= , CM000677.2:g.73332178G= GRCh38
NC_000015.9:g.73624519G= , CM000677.1:g.73624519G= GRCh37
NC_000015.8:g.71411572G= NCBI36
NG_009063.1:g.42087C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1324C= MANE Select ENSP00000261917.3:p.Leu442=
ENST00000261917.3:c.1324C= ENSP00000261917.3:p.Leu442=
NM_005477.2:c.1324C= NP_005468.1:p.Leu442=
XM_011521148.1:c.106C= XP_011519450.1:p.Leu36=
XM_011521148.2:c.106C= XP_011519450.1:p.Leu36=
NM_005477.3:c.1324C= MANE Select NP_005468.1:p.Leu442=