Canonical Allele Identifier: CA2187167942
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73330097G= , CM000677.2:g.73330097G= GRCh38
NC_000015.9:g.73622438G= , CM000677.1:g.73622438G= GRCh37
NC_000015.8:g.71409491G= NCBI36
NG_009063.1:g.44168C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1372-306C= MANE Select ENSP00000261917.3:n.1372-306C=
ENST00000261917.3:c.1372-306C= ENSP00000261917.3:n.1372-306C=
NM_005477.2:c.1372-306C= NP_005468.1:n.1372-306C=
XM_011521148.1:c.154-306C= XP_011519450.1:n.154-306C=
XM_011521148.2:c.154-306C= XP_011519450.1:n.154-306C=
NM_005477.3:c.1372-306C= MANE Select NP_005468.1:n.1372-306C=
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