Canonical Allele Identifier: CA393086003
Gene: HCN4 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322882T>A , CM000677.2:g.73322882T>A GRCh38
NC_000015.9:g.73615223T>A , CM000677.1:g.73615223T>A GRCh37
NC_000015.8:g.71402276T>A NCBI36
NG_009063.1:g.51383A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3211A>T MANE Select ENSP00000261917.3:p.Thr1071Ser
ENST00000261917.3:c.3211A>T ENSP00000261917.3:p.Thr1071Ser
NM_005477.2:c.3211A>T NP_005468.1:p.Thr1071Ser
XM_011521148.1:c.1993A>T XP_011519450.1:p.Thr665Ser
XM_011521148.2:c.1993A>T XP_011519450.1:p.Thr665Ser
NM_005477.3:c.3211A>T MANE Select NP_005468.1:p.Thr1071Ser