Canonical Allele Identifier: CA2187186351
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322643G= , CM000677.2:g.73322643G= GRCh38
NC_000015.9:g.73614984G= , CM000677.1:g.73614984G= GRCh37
NC_000015.8:g.71402037G= NCBI36
NG_009063.1:g.51622C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3450C= MANE Select ENSP00000261917.3:p.Val1150=
ENST00000261917.3:c.3450C= ENSP00000261917.3:p.Val1150=
NM_005477.2:c.3450C= NP_005468.1:p.Val1150=
XM_011521148.1:c.2232C= XP_011519450.1:p.Val744=
XM_011521148.2:c.2232C= XP_011519450.1:p.Val744=
NM_005477.3:c.3450C= MANE Select NP_005468.1:p.Val1150=