Canonical Allele Identifier: CA2187194602
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367900T= , CM000677.2:g.73367900T= GRCh38
NC_000015.9:g.73660241T= , CM000677.1:g.73660241T= GRCh37
NC_000015.8:g.71447294T= NCBI36
NG_009063.1:g.6365A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.371A= MANE Select ENSP00000261917.3:p.Asp124=
ENST00000261917.3:c.371A= ENSP00000261917.3:p.Asp124=
NM_005477.2:c.371A= NP_005468.1:p.Asp124=
NM_005477.3:c.371A= MANE Select NP_005468.1:p.Asp124=
Search 100 bp 5'
Search 100 bp 3'