Canonical Allele Identifier: CA393087094
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2008533
ClinVar RCV Id: RCV002828688

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323208G>A , CM000677.2:g.73323208G>A GRCh38
NC_000015.9:g.73615549G>A , CM000677.1:g.73615549G>A GRCh37
NC_000015.8:g.71402602G>A NCBI36
NG_009063.1:g.51057C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2885C>T MANE Select ENSP00000261917.3:p.Pro962Leu
ENST00000261917.3:c.2885C>T ENSP00000261917.3:p.Pro962Leu
NM_005477.2:c.2885C>T NP_005468.1:p.Pro962Leu
XM_011521148.1:c.1667C>T XP_011519450.1:p.Pro556Leu
XM_011521148.2:c.1667C>T XP_011519450.1:p.Pro556Leu
NM_005477.3:c.2885C>T MANE Select NP_005468.1:p.Pro962Leu