Canonical Allele Identifier: CA16607014
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 388974
dbSNP Id: rs146954200

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73343604C>A , CM000677.2:g.73343604C>A GRCh38
NC_000015.9:g.73635945C>A , CM000677.1:g.73635945C>A GRCh37
NC_000015.8:g.71422998C>A NCBI36
NG_009063.1:g.30661G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.990G>T MANE Select ENSP00000261917.3:p.Pro330=
ENST00000261917.3:c.990G>T ENSP00000261917.3:p.Pro330=
NM_005477.2:c.990G>T NP_005468.1:p.Pro330=
NM_005477.3:c.990G>T MANE Select NP_005468.1:p.Pro330=