Canonical Allele Identifier: CA2187180052
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73343642T= , CM000677.2:g.73343642T= GRCh38
NC_000015.9:g.73635983T= , CM000677.1:g.73635983T= GRCh37
NC_000015.8:g.71423036T= NCBI36
NG_009063.1:g.30623A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.952A= MANE Select ENSP00000261917.3:p.Ile318=
ENST00000261917.3:c.952A= ENSP00000261917.3:p.Ile318=
NM_005477.2:c.952A= NP_005468.1:p.Ile318=
NM_005477.3:c.952A= MANE Select NP_005468.1:p.Ile318=
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