Canonical Allele Identifier: CA2187187709
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323206G= , CM000677.2:g.73323206G= GRCh38
NC_000015.9:g.73615547G= , CM000677.1:g.73615547G= GRCh37
NC_000015.8:g.71402600G= NCBI36
NG_009063.1:g.51059C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2887C= MANE Select ENSP00000261917.3:p.Pro963=
ENST00000261917.3:c.2887C= ENSP00000261917.3:p.Pro963=
NM_005477.2:c.2887C= NP_005468.1:p.Pro963=
XM_011521148.1:c.1669C= XP_011519450.1:p.Pro557=
XM_011521148.2:c.1669C= XP_011519450.1:p.Pro557=
NM_005477.3:c.2887C= MANE Select NP_005468.1:p.Pro963=