Canonical Allele Identifier: CA2187187632
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323175C= , CM000677.2:g.73323175C= GRCh38
NC_000015.9:g.73615516C= , CM000677.1:g.73615516C= GRCh37
NC_000015.8:g.71402569C= NCBI36
NG_009063.1:g.51090G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2918G= MANE Select ENSP00000261917.3:p.Gly973=
ENST00000261917.3:c.2918G= ENSP00000261917.3:p.Gly973=
NM_005477.2:c.2918G= NP_005468.1:p.Gly973=
XM_011521148.1:c.1700G= XP_011519450.1:p.Gly567=
XM_011521148.2:c.1700G= XP_011519450.1:p.Gly567=
NM_005477.3:c.2918G= MANE Select NP_005468.1:p.Gly973=