Canonical Allele Identifier: CA2629388772
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332024A>G , CM000677.2:g.73332024A>G GRCh38
NC_000015.9:g.73624365A>G , CM000677.1:g.73624365A>G GRCh37
NC_000015.8:g.71411418A>G NCBI36
NG_009063.1:g.42241T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1371+107T>C MANE Select ENSP00000261917.3:n.1371+107T>C
ENST00000261917.3:c.1371+107T>C ENSP00000261917.3:n.1371+107T>C
NM_005477.2:c.1371+107T>C NP_005468.1:n.1371+107T>C
XM_011521148.1:c.153+107T>C XP_011519450.1:n.153+107T>C
XM_011521148.2:c.153+107T>C XP_011519450.1:n.153+107T>C
NM_005477.3:c.1371+107T>C MANE Select NP_005468.1:n.1371+107T>C