Canonical Allele Identifier: CA393094139
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs2042922121

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329772T>C , CM000677.2:g.73329772T>C GRCh38
NC_000015.9:g.73622113T>C , CM000677.1:g.73622113T>C GRCh37
NC_000015.8:g.71409166T>C NCBI36
NG_009063.1:g.44493A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1391A>G MANE Select ENSP00000261917.3:p.Gln464Arg
ENST00000261917.3:c.1391A>G ENSP00000261917.3:p.Gln464Arg
NM_005477.2:c.1391A>G NP_005468.1:p.Gln464Arg
XM_011521148.1:c.173A>G XP_011519450.1:p.Gln58Arg
XM_011521148.2:c.173A>G XP_011519450.1:p.Gln58Arg
NM_005477.3:c.1391A>G MANE Select NP_005468.1:p.Gln464Arg