Canonical Allele Identifier: CA2575783797
Gene: HCN4 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322391T>C , CM000677.2:g.73322391T>C GRCh38
NC_000015.9:g.73614732T>C , CM000677.1:g.73614732T>C GRCh37
NC_000015.8:g.71401785T>C NCBI36
NG_009063.1:g.51874A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.*90A>G MANE Select ENSP00000261917.3:n.*90A>G
ENST00000261917.3:c.*90A>G ENSP00000261917.3:n.*90A>G
NM_005477.2:c.*90A>G NP_005468.1:n.*90A>G
XM_011521148.1:c.*90A>G XP_011519450.1:n.*90A>G
XM_011521148.2:c.*90A>G XP_011519450.1:n.*90A>G
NM_005477.3:c.*90A>G MANE Select NP_005468.1:n.*90A>G
Search 100 bp 5'
Search 100 bp 3'