Canonical Allele Identifier: CA2629388770
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332022T>C , CM000677.2:g.73332022T>C GRCh38
NC_000015.9:g.73624363T>C , CM000677.1:g.73624363T>C GRCh37
NC_000015.8:g.71411416T>C NCBI36
NG_009063.1:g.42243A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1371+109A>G MANE Select ENSP00000261917.3:n.1371+109A>G
ENST00000261917.3:c.1371+109A>G ENSP00000261917.3:n.1371+109A>G
NM_005477.2:c.1371+109A>G NP_005468.1:n.1371+109A>G
XM_011521148.1:c.153+109A>G XP_011519450.1:n.153+109A>G
XM_011521148.2:c.153+109A>G XP_011519450.1:n.153+109A>G
NM_005477.3:c.1371+109A>G MANE Select NP_005468.1:n.1371+109A>G