Canonical Allele Identifier: CA2187167319
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329523G= , CM000677.2:g.73329523G= GRCh38
NC_000015.9:g.73621864G= , CM000677.1:g.73621864G= GRCh37
NC_000015.8:g.71408917G= NCBI36
NG_009063.1:g.44742C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1590+50C= MANE Select ENSP00000261917.3:n.1590+50C=
ENST00000261917.3:c.1590+50C= ENSP00000261917.3:n.1590+50C=
NM_005477.2:c.1590+50C= NP_005468.1:n.1590+50C=
XM_011521148.1:c.372+50C= XP_011519450.1:n.372+50C=
XM_011521148.2:c.372+50C= XP_011519450.1:n.372+50C=
NM_005477.3:c.1590+50C= MANE Select NP_005468.1:n.1590+50C=
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