Canonical Allele Identifier: CA2629370520
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322479G>T , CM000677.2:g.73322479G>T GRCh38
NC_000015.9:g.73614820G>T , CM000677.1:g.73614820G>T GRCh37
NC_000015.8:g.71401873G>T NCBI36
NG_009063.1:g.51786C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.*2C>A MANE Select ENSP00000261917.3:n.*2C>A
ENST00000261917.3:c.*2C>A ENSP00000261917.3:n.*2C>A
NM_005477.2:c.*2C>A NP_005468.1:n.*2C>A
XM_011521148.1:c.*2C>A XP_011519450.1:n.*2C>A
XM_011521148.2:c.*2C>A XP_011519450.1:n.*2C>A
NM_005477.3:c.*2C>A MANE Select NP_005468.1:n.*2C>A