Canonical Allele Identifier: CA2187167893
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73330034T= , CM000677.2:g.73330034T= GRCh38
NC_000015.9:g.73622375T= , CM000677.1:g.73622375T= GRCh37
NC_000015.8:g.71409428T= NCBI36
NG_009063.1:g.44231A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1372-243A= MANE Select ENSP00000261917.3:n.1372-243A=
ENST00000261917.3:c.1372-243A= ENSP00000261917.3:n.1372-243A=
NM_005477.2:c.1372-243A= NP_005468.1:n.1372-243A=
XM_011521148.1:c.154-243A= XP_011519450.1:n.154-243A=
XM_011521148.2:c.154-243A= XP_011519450.1:n.154-243A=
NM_005477.3:c.1372-243A= MANE Select NP_005468.1:n.1372-243A=
Search 100 bp 5'
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