Canonical Allele Identifier: CA2629388788
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332052T>A , CM000677.2:g.73332052T>A GRCh38
NC_000015.9:g.73624393T>A , CM000677.1:g.73624393T>A GRCh37
NC_000015.8:g.71411446T>A NCBI36
NG_009063.1:g.42213A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1371+79A>T MANE Select ENSP00000261917.3:n.1371+79A>T
ENST00000261917.3:c.1371+79A>T ENSP00000261917.3:n.1371+79A>T
NM_005477.2:c.1371+79A>T NP_005468.1:n.1371+79A>T
XM_011521148.1:c.153+79A>T XP_011519450.1:n.153+79A>T
XM_011521148.2:c.153+79A>T XP_011519450.1:n.153+79A>T
NM_005477.3:c.1371+79A>T MANE Select NP_005468.1:n.1371+79A>T