Canonical Allele Identifier: CA2575784040
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73368288-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368288T>C , CM000677.2:g.73368288T>C GRCh38
NC_000015.9:g.73660629T>C , CM000677.1:g.73660629T>C GRCh37
NC_000015.8:g.71447682T>C NCBI36
NG_009063.1:g.5977A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.-18A>G MANE Select ENSP00000261917.3:n.-18A>G
ENST00000261917.3:c.-18A>G ENSP00000261917.3:n.-18A>G
NM_005477.2:c.-18A>G NP_005468.1:n.-18A>G
NM_005477.3:c.-18A>G MANE Select NP_005468.1:n.-18A>G
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