Canonical Allele Identifier: CA393094105
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329764A>T , CM000677.2:g.73329764A>T GRCh38
NC_000015.9:g.73622105A>T , CM000677.1:g.73622105A>T GRCh37
NC_000015.8:g.71409158A>T NCBI36
NG_009063.1:g.44501T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1399T>A MANE Select ENSP00000261917.3:p.Tyr467Asn
ENST00000261917.3:c.1399T>A ENSP00000261917.3:p.Tyr467Asn
NM_005477.2:c.1399T>A NP_005468.1:p.Tyr467Asn
XM_011521148.1:c.181T>A XP_011519450.1:p.Tyr61Asn
XM_011521148.2:c.181T>A XP_011519450.1:p.Tyr61Asn
NM_005477.3:c.1399T>A MANE Select NP_005468.1:p.Tyr467Asn