Canonical Allele Identifier: CA2187194463
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367608C= , CM000677.2:g.73367608C= GRCh38
NC_000015.9:g.73659949C= , CM000677.1:g.73659949C= GRCh37
NC_000015.8:g.71447002C= NCBI36
NG_009063.1:g.6657G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.663G= MANE Select ENSP00000261917.3:p.Met221=
ENST00000261917.3:c.663G= ENSP00000261917.3:p.Met221=
NM_005477.2:c.663G= NP_005468.1:p.Met221=
NM_005477.3:c.663G= MANE Select NP_005468.1:p.Met221=
Search 100 bp 5'
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