Canonical Allele Identifier: CA393097392
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367632G>C , CM000677.2:g.73367632G>C GRCh38
NC_000015.9:g.73659973G>C , CM000677.1:g.73659973G>C GRCh37
NC_000015.8:g.71447026G>C NCBI36
NG_009063.1:g.6633C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.639C>G MANE Select ENSP00000261917.3:p.Phe213Leu
ENST00000261917.3:c.639C>G ENSP00000261917.3:p.Phe213Leu
NM_005477.2:c.639C>G NP_005468.1:p.Phe213Leu
NM_005477.3:c.639C>G MANE Select NP_005468.1:p.Phe213Leu