Canonical Allele Identifier: CA2187185906
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322410A= , CM000677.2:g.73322410A= GRCh38
NC_000015.9:g.73614751A= , CM000677.1:g.73614751A= GRCh37
NC_000015.8:g.71401804A= NCBI36
NG_009063.1:g.51855T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.*71T= MANE Select ENSP00000261917.3:n.*71T=
ENST00000261917.3:c.*71T= ENSP00000261917.3:n.*71T=
NM_005477.2:c.*71T= NP_005468.1:n.*71T=
XM_011521148.1:c.*71T= XP_011519450.1:n.*71T=
XM_011521148.2:c.*71T= XP_011519450.1:n.*71T=
NM_005477.3:c.*71T= MANE Select NP_005468.1:n.*71T=
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