Canonical Allele Identifier: CA393098077
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367850C>G , CM000677.2:g.73367850C>G GRCh38
NC_000015.9:g.73660191C>G , CM000677.1:g.73660191C>G GRCh37
NC_000015.8:g.71447244C>G NCBI36
NG_009063.1:g.6415G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.421G>C MANE Select ENSP00000261917.3:p.Glu141Gln
ENST00000261917.3:c.421G>C ENSP00000261917.3:p.Glu141Gln
NM_005477.2:c.421G>C NP_005468.1:p.Glu141Gln
NM_005477.3:c.421G>C MANE Select NP_005468.1:p.Glu141Gln