Canonical Allele Identifier: CA393098751
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368078T>A , CM000677.2:g.73368078T>A GRCh38
NC_000015.9:g.73660419T>A , CM000677.1:g.73660419T>A GRCh37
NC_000015.8:g.71447472T>A NCBI36
NG_009063.1:g.6187A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.193A>T MANE Select ENSP00000261917.3:p.Thr65Ser
ENST00000261917.3:c.193A>T ENSP00000261917.3:p.Thr65Ser
NM_005477.2:c.193A>T NP_005468.1:p.Thr65Ser
NM_005477.3:c.193A>T MANE Select NP_005468.1:p.Thr65Ser