Canonical Allele Identifier: CA2187169611
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1567776871
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332056A>T , CM000677.2:g.73332056A>T GRCh38
NC_000015.9:g.73624397A>T , CM000677.1:g.73624397A>T GRCh37
NC_000015.8:g.71411450A>T NCBI36
NG_009063.1:g.42209T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1371+75T>A MANE Select ENSP00000261917.3:n.1371+75T>A
ENST00000261917.3:c.1371+75T>A ENSP00000261917.3:n.1371+75T>A
NM_005477.2:c.1371+75T>A NP_005468.1:n.1371+75T>A
XM_011521148.1:c.153+75T>A XP_011519450.1:n.153+75T>A
XM_011521148.2:c.153+75T>A XP_011519450.1:n.153+75T>A
NM_005477.3:c.1371+75T>A MANE Select NP_005468.1:n.1371+75T>A
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