Canonical Allele Identifier: CA393098082
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367852C>T , CM000677.2:g.73367852C>T GRCh38
NC_000015.9:g.73660193C>T , CM000677.1:g.73660193C>T GRCh37
NC_000015.8:g.71447246C>T NCBI36
NG_009063.1:g.6413G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.419G>A MANE Select ENSP00000261917.3:p.Gly140Asp
ENST00000261917.3:c.419G>A ENSP00000261917.3:p.Gly140Asp
NM_005477.2:c.419G>A NP_005468.1:p.Gly140Asp
NM_005477.3:c.419G>A MANE Select NP_005468.1:p.Gly140Asp