Canonical Allele Identifier: CA272663408
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1354312
dbSNP Id: rs940405280

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322776G>A , CM000677.2:g.73322776G>A GRCh38
NC_000015.9:g.73615117G>A , CM000677.1:g.73615117G>A GRCh37
NC_000015.8:g.71402170G>A NCBI36
NG_009063.1:g.51489C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3317C>T MANE Select ENSP00000261917.3:p.Pro1106Leu
ENST00000261917.3:c.3317C>T ENSP00000261917.3:p.Pro1106Leu
NM_005477.2:c.3317C>T NP_005468.1:p.Pro1106Leu
XM_011521148.1:c.2099C>T XP_011519450.1:p.Pro700Leu
XM_011521148.2:c.2099C>T XP_011519450.1:p.Pro700Leu
NM_005477.3:c.3317C>T MANE Select NP_005468.1:p.Pro1106Leu