Canonical Allele Identifier: CA2629388698
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73329932-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329932G>C , CM000677.2:g.73329932G>C GRCh38
NC_000015.9:g.73622273G>C , CM000677.1:g.73622273G>C GRCh37
NC_000015.8:g.71409326G>C NCBI36
NG_009063.1:g.44333C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1372-141C>G MANE Select ENSP00000261917.3:n.1372-141C>G
ENST00000261917.3:c.1372-141C>G ENSP00000261917.3:n.1372-141C>G
NM_005477.2:c.1372-141C>G NP_005468.1:n.1372-141C>G
XM_011521148.1:c.154-141C>G XP_011519450.1:n.154-141C>G
XM_011521148.2:c.154-141C>G XP_011519450.1:n.154-141C>G
NM_005477.3:c.1372-141C>G MANE Select NP_005468.1:n.1372-141C>G
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