Canonical Allele Identifier: CA393098026
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367835G>C , CM000677.2:g.73367835G>C GRCh38
NC_000015.9:g.73660176G>C , CM000677.1:g.73660176G>C GRCh37
NC_000015.8:g.71447229G>C NCBI36
NG_009063.1:g.6430C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.436C>G MANE Select ENSP00000261917.3:p.Pro146Ala
ENST00000261917.3:c.436C>G ENSP00000261917.3:p.Pro146Ala
NM_005477.2:c.436C>G NP_005468.1:p.Pro146Ala
NM_005477.3:c.436C>G MANE Select NP_005468.1:p.Pro146Ala