Canonical Allele Identifier: CA2187194795
Gene: HCN4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368251G= , CM000677.2:g.73368251G= GRCh38
NC_000015.9:g.73660592G= , CM000677.1:g.73660592G= GRCh37
NC_000015.8:g.71447645G= NCBI36
NG_009063.1:g.6014C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.20C= MANE Select ENSP00000261917.3:p.Ser7=
ENST00000261917.3:c.20C= ENSP00000261917.3:p.Ser7=
NM_005477.2:c.20C= NP_005468.1:p.Ser7=
NM_005477.3:c.20C= MANE Select NP_005468.1:p.Ser7=
Search 100 bp 5'
Search 100 bp 3'