Canonical Allele Identifier: CA393093795
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329689C>A , CM000677.2:g.73329689C>A GRCh38
NC_000015.9:g.73622030C>A , CM000677.1:g.73622030C>A GRCh37
NC_000015.8:g.71409083C>A NCBI36
NG_009063.1:g.44576G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1474G>T MANE Select ENSP00000261917.3:p.Val492Phe
ENST00000261917.3:c.1474G>T ENSP00000261917.3:p.Val492Phe
NM_005477.2:c.1474G>T NP_005468.1:p.Val492Phe
XM_011521148.1:c.256G>T XP_011519450.1:p.Val86Phe
XM_011521148.2:c.256G>T XP_011519450.1:p.Val86Phe
NM_005477.3:c.1474G>T MANE Select NP_005468.1:p.Val492Phe