Canonical Allele Identifier: CA393097836
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367772G>A , CM000677.2:g.73367772G>A GRCh38
NC_000015.9:g.73660113G>A , CM000677.1:g.73660113G>A GRCh37
NC_000015.8:g.71447166G>A NCBI36
NG_009063.1:g.6493C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.499C>T MANE Select ENSP00000261917.3:p.Pro167Ser
ENST00000261917.3:c.499C>T ENSP00000261917.3:p.Pro167Ser
NM_005477.2:c.499C>T NP_005468.1:p.Pro167Ser
NM_005477.3:c.499C>T MANE Select NP_005468.1:p.Pro167Ser