Canonical Allele Identifier: CA2187194544
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367765T= , CM000677.2:g.73367765T= GRCh38
NC_000015.9:g.73660106T= , CM000677.1:g.73660106T= GRCh37
NC_000015.8:g.71447159T= NCBI36
NG_009063.1:g.6500A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.506A= MANE Select ENSP00000261917.3:p.Gln169=
ENST00000261917.3:c.506A= ENSP00000261917.3:p.Gln169=
NM_005477.2:c.506A= NP_005468.1:p.Gln169=
NM_005477.3:c.506A= MANE Select NP_005468.1:p.Gln169=
Search 100 bp 5'
Search 100 bp 3'