Canonical Allele Identifier: CA2629388584
Gene: HCN4 HGNC NCBI

Linked Data

gnomAD v4: 15-73329565-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329565A>C , CM000677.2:g.73329565A>C GRCh38
NC_000015.9:g.73621906A>C , CM000677.1:g.73621906A>C GRCh37
NC_000015.8:g.71408959A>C NCBI36
NG_009063.1:g.44700T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1590+8T>G MANE Select ENSP00000261917.3:n.1590+8T>G
ENST00000261917.3:c.1590+8T>G ENSP00000261917.3:n.1590+8T>G
NM_005477.2:c.1590+8T>G NP_005468.1:n.1590+8T>G
XM_011521148.1:c.372+8T>G XP_011519450.1:n.372+8T>G
XM_011521148.2:c.372+8T>G XP_011519450.1:n.372+8T>G
NM_005477.3:c.1590+8T>G MANE Select NP_005468.1:n.1590+8T>G
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