Canonical Allele Identifier: CA2629388783
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332043C>A , CM000677.2:g.73332043C>A GRCh38
NC_000015.9:g.73624384C>A , CM000677.1:g.73624384C>A GRCh37
NC_000015.8:g.71411437C>A NCBI36
NG_009063.1:g.42222G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1371+88G>T MANE Select ENSP00000261917.3:n.1371+88G>T
ENST00000261917.3:c.1371+88G>T ENSP00000261917.3:n.1371+88G>T
NM_005477.2:c.1371+88G>T NP_005468.1:n.1371+88G>T
XM_011521148.1:c.153+88G>T XP_011519450.1:n.153+88G>T
XM_011521148.2:c.153+88G>T XP_011519450.1:n.153+88G>T
NM_005477.3:c.1371+88G>T MANE Select NP_005468.1:n.1371+88G>T