Canonical Allele Identifier: CA2187194587
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367861G= , CM000677.2:g.73367861G= GRCh38
NC_000015.9:g.73660202G= , CM000677.1:g.73660202G= GRCh37
NC_000015.8:g.71447255G= NCBI36
NG_009063.1:g.6404C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.410C= MANE Select ENSP00000261917.3:p.Ala137=
ENST00000261917.3:c.410C= ENSP00000261917.3:p.Ala137=
NM_005477.2:c.410C= NP_005468.1:p.Ala137=
NM_005477.3:c.410C= MANE Select NP_005468.1:p.Ala137=