Canonical Allele Identifier: CA2629389918
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73368287-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368287G>T , CM000677.2:g.73368287G>T GRCh38
NC_000015.9:g.73660628G>T , CM000677.1:g.73660628G>T GRCh37
NC_000015.8:g.71447681G>T NCBI36
NG_009063.1:g.5978C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.-17C>A MANE Select ENSP00000261917.3:n.-17C>A
ENST00000261917.3:c.-17C>A ENSP00000261917.3:n.-17C>A
NM_005477.2:c.-17C>A NP_005468.1:n.-17C>A
NM_005477.3:c.-17C>A MANE Select NP_005468.1:n.-17C>A
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