Canonical Allele Identifier: CA393098080
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.419G>T MANE Select ENSP00000261917.3:p.Gly140Val
ENST00000261917.3:c.419G>T ENSP00000261917.3:p.Gly140Val
NM_005477.2:c.419G>T NP_005468.1:p.Gly140Val
NM_005477.3:c.419G>T MANE Select NP_005468.1:p.Gly140Val