Canonical Allele Identifier: CA2187180055
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73343648T= , CM000677.2:g.73343648T= GRCh38
NC_000015.9:g.73635989T= , CM000677.1:g.73635989T= GRCh37
NC_000015.8:g.71423042T= NCBI36
NG_009063.1:g.30617A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.946A= MANE Select ENSP00000261917.3:p.Thr316=
ENST00000261917.3:c.946A= ENSP00000261917.3:p.Thr316=
NM_005477.2:c.946A= NP_005468.1:p.Thr316=
NM_005477.3:c.946A= MANE Select NP_005468.1:p.Thr316=
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