Canonical Allele Identifier: CA2187167978
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73330123C= , CM000677.2:g.73330123C= GRCh38
NC_000015.9:g.73622464C= , CM000677.1:g.73622464C= GRCh37
NC_000015.8:g.71409517C= NCBI36
NG_009063.1:g.44142G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1372-332G= MANE Select ENSP00000261917.3:n.1372-332G=
ENST00000261917.3:c.1372-332G= ENSP00000261917.3:n.1372-332G=
NM_005477.2:c.1372-332G= NP_005468.1:n.1372-332G=
XM_011521148.1:c.154-332G= XP_011519450.1:n.154-332G=
XM_011521148.2:c.154-332G= XP_011519450.1:n.154-332G=
NM_005477.3:c.1372-332G= MANE Select NP_005468.1:n.1372-332G=
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