Canonical Allele Identifier: CA2187194811
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368276C= , CM000677.2:g.73368276C= GRCh38
NC_000015.9:g.73660617C= , CM000677.1:g.73660617C= GRCh37
NC_000015.8:g.71447670C= NCBI36
NG_009063.1:g.5989G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.-6G= MANE Select ENSP00000261917.3:n.-6G=
ENST00000261917.3:c.-6G= ENSP00000261917.3:n.-6G=
NM_005477.2:c.-6G= NP_005468.1:n.-6G=
NM_005477.3:c.-6G= MANE Select NP_005468.1:n.-6G=
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