Canonical Allele Identifier: CA2629388792
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73332058-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332058T>C , CM000677.2:g.73332058T>C GRCh38
NC_000015.9:g.73624399T>C , CM000677.1:g.73624399T>C GRCh37
NC_000015.8:g.71411452T>C NCBI36
NG_009063.1:g.42207A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1371+73A>G MANE Select ENSP00000261917.3:n.1371+73A>G
ENST00000261917.3:c.1371+73A>G ENSP00000261917.3:n.1371+73A>G
NM_005477.2:c.1371+73A>G NP_005468.1:n.1371+73A>G
XM_011521148.1:c.153+73A>G XP_011519450.1:n.153+73A>G
XM_011521148.2:c.153+73A>G XP_011519450.1:n.153+73A>G
NM_005477.3:c.1371+73A>G MANE Select NP_005468.1:n.1371+73A>G
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