Canonical Allele Identifier: CA393088621
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323516G>C , CM000677.2:g.73323516G>C GRCh38
NC_000015.9:g.73615857G>C , CM000677.1:g.73615857G>C GRCh37
NC_000015.8:g.71402910G>C NCBI36
NG_009063.1:g.50749C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2577C>G MANE Select ENSP00000261917.3:p.Ile859Met
ENST00000261917.3:c.2577C>G ENSP00000261917.3:p.Ile859Met
NM_005477.2:c.2577C>G NP_005468.1:p.Ile859Met
XM_011521148.1:c.1359C>G XP_011519450.1:p.Ile453Met
XM_011521148.2:c.1359C>G XP_011519450.1:p.Ile453Met
NM_005477.3:c.2577C>G MANE Select NP_005468.1:p.Ile859Met