Canonical Allele Identifier: CA2187194488
Gene: HCN4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367665C= , CM000677.2:g.73367665C= GRCh38
NC_000015.9:g.73660006C= , CM000677.1:g.73660006C= GRCh37
NC_000015.8:g.71447059C= NCBI36
NG_009063.1:g.6600G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.606G= MANE Select ENSP00000261917.3:p.Pro202=
ENST00000261917.3:c.606G= ENSP00000261917.3:p.Pro202=
NM_005477.2:c.606G= NP_005468.1:p.Pro202=
NM_005477.3:c.606G= MANE Select NP_005468.1:p.Pro202=
Search 100 bp 5'
Search 100 bp 3'