Canonical Allele Identifier: CA2187194692
Gene: HCN4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368059G= , CM000677.2:g.73368059G= GRCh38
NC_000015.9:g.73660400G= , CM000677.1:g.73660400G= GRCh37
NC_000015.8:g.71447453G= NCBI36
NG_009063.1:g.6206C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.212C= MANE Select ENSP00000261917.3:p.Ala71=
ENST00000261917.3:c.212C= ENSP00000261917.3:p.Ala71=
NM_005477.2:c.212C= NP_005468.1:p.Ala71=
NM_005477.3:c.212C= MANE Select NP_005468.1:p.Ala71=
Search 100 bp 5'
Search 100 bp 3'