Canonical Allele Identifier: CA2187186441
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322684G= , CM000677.2:g.73322684G= GRCh38
NC_000015.9:g.73615025G= , CM000677.1:g.73615025G= GRCh37
NC_000015.8:g.71402078G= NCBI36
NG_009063.1:g.51581C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3409C= MANE Select ENSP00000261917.3:p.Pro1137=
ENST00000261917.3:c.3409C= ENSP00000261917.3:p.Pro1137=
NM_005477.2:c.3409C= NP_005468.1:p.Pro1137=
XM_011521148.1:c.2191C= XP_011519450.1:p.Pro731=
XM_011521148.2:c.2191C= XP_011519450.1:p.Pro731=
NM_005477.3:c.3409C= MANE Select NP_005468.1:p.Pro1137=