Canonical Allele Identifier: CA393093817
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329697A>C , CM000677.2:g.73329697A>C GRCh38
NC_000015.9:g.73622038A>C , CM000677.1:g.73622038A>C GRCh37
NC_000015.8:g.71409091A>C NCBI36
NG_009063.1:g.44568T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1466T>G MANE Select ENSP00000261917.3:p.Met489Arg
ENST00000261917.3:c.1466T>G ENSP00000261917.3:p.Met489Arg
NM_005477.2:c.1466T>G NP_005468.1:p.Met489Arg
XM_011521148.1:c.248T>G XP_011519450.1:p.Met83Arg
XM_011521148.2:c.248T>G XP_011519450.1:p.Met83Arg
NM_005477.3:c.1466T>G MANE Select NP_005468.1:p.Met489Arg