Canonical Allele Identifier: CA7648928
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2984583
ClinVar RCV Id: RCV003845726
dbSNP Id: rs773256230

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323186T>C , CM000677.2:g.73323186T>C GRCh38
NC_000015.9:g.73615527T>C , CM000677.1:g.73615527T>C GRCh37
NC_000015.8:g.71402580T>C NCBI36
NG_009063.1:g.51079A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.2907A>G MANE Select ENSP00000261917.3:p.Ser969=
ENST00000261917.3:c.2907A>G ENSP00000261917.3:p.Ser969=
NM_005477.2:c.2907A>G NP_005468.1:p.Ser969=
XM_011521148.1:c.1689A>G XP_011519450.1:p.Ser563=
XM_011521148.2:c.1689A>G XP_011519450.1:p.Ser563=
NM_005477.3:c.2907A>G MANE Select NP_005468.1:p.Ser969=