Canonical Allele Identifier: CA16043943
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 374860
dbSNP Id: rs1057519275

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329722A>G , CM000677.2:g.73329722A>G GRCh38
NC_000015.9:g.73622063A>G , CM000677.1:g.73622063A>G GRCh37
NC_000015.8:g.71409116A>G NCBI36
NG_009063.1:g.44543T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1441T>C MANE Select ENSP00000261917.3:p.Tyr481His
ENST00000261917.3:c.1441T>C ENSP00000261917.3:p.Tyr481His
NM_005477.2:c.1441T>C NP_005468.1:p.Tyr481His
XM_011521148.1:c.223T>C XP_011519450.1:p.Tyr75His
XM_011521148.2:c.223T>C XP_011519450.1:p.Tyr75His
NM_005477.3:c.1441T>C MANE Select NP_005468.1:p.Tyr481His