Canonical Allele Identifier: CA491478660
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs1186075319

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323450G>A , CM000677.2:g.73323450G>A GRCh38
NC_000015.9:g.73615791G>A , CM000677.1:g.73615791G>A GRCh37
NC_000015.8:g.71402844G>A NCBI36
NG_009063.1:g.50815C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2643C>T MANE Select ENSP00000261917.3:p.Ser881=
ENST00000261917.3:c.2643C>T ENSP00000261917.3:p.Ser881=
NM_005477.2:c.2643C>T NP_005468.1:p.Ser881=
XM_011521148.1:c.1425C>T XP_011519450.1:p.Ser475=
XM_011521148.2:c.1425C>T XP_011519450.1:p.Ser475=
NM_005477.3:c.2643C>T MANE Select NP_005468.1:p.Ser881=