Canonical Allele Identifier: CA393097972
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367817G>T , CM000677.2:g.73367817G>T GRCh38
NC_000015.9:g.73660158G>T , CM000677.1:g.73660158G>T GRCh37
NC_000015.8:g.71447211G>T NCBI36
NG_009063.1:g.6448C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.454C>A MANE Select ENSP00000261917.3:p.Pro152Thr
ENST00000261917.3:c.454C>A ENSP00000261917.3:p.Pro152Thr
NM_005477.2:c.454C>A NP_005468.1:p.Pro152Thr
NM_005477.3:c.454C>A MANE Select NP_005468.1:p.Pro152Thr