Canonical Allele Identifier: CA2187167952
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73330103G= , CM000677.2:g.73330103G= GRCh38
NC_000015.9:g.73622444G= , CM000677.1:g.73622444G= GRCh37
NC_000015.8:g.71409497G= NCBI36
NG_009063.1:g.44162C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1372-312C= MANE Select ENSP00000261917.3:n.1372-312C=
ENST00000261917.3:c.1372-312C= ENSP00000261917.3:n.1372-312C=
NM_005477.2:c.1372-312C= NP_005468.1:n.1372-312C=
XM_011521148.1:c.154-312C= XP_011519450.1:n.154-312C=
XM_011521148.2:c.154-312C= XP_011519450.1:n.154-312C=
NM_005477.3:c.1372-312C= MANE Select NP_005468.1:n.1372-312C=
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