Canonical Allele Identifier: CA393086114
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322941G>T , CM000677.2:g.73322941G>T GRCh38
NC_000015.9:g.73615282G>T , CM000677.1:g.73615282G>T GRCh37
NC_000015.8:g.71402335G>T NCBI36
NG_009063.1:g.51324C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3152C>A MANE Select ENSP00000261917.3:p.Ser1051Tyr
ENST00000261917.3:c.3152C>A ENSP00000261917.3:p.Ser1051Tyr
NM_005477.2:c.3152C>A NP_005468.1:p.Ser1051Tyr
XM_011521148.1:c.1934C>A XP_011519450.1:p.Ser645Tyr
XM_011521148.2:c.1934C>A XP_011519450.1:p.Ser645Tyr
NM_005477.3:c.3152C>A MANE Select NP_005468.1:p.Ser1051Tyr