Canonical Allele Identifier: CA2187186213
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322552T= , CM000677.2:g.73322552T= GRCh38
NC_000015.9:g.73614893T= , CM000677.1:g.73614893T= GRCh37
NC_000015.8:g.71401946T= NCBI36
NG_009063.1:g.51713A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3541A= MANE Select ENSP00000261917.3:p.Thr1181=
ENST00000261917.3:c.3541A= ENSP00000261917.3:p.Thr1181=
NM_005477.2:c.3541A= NP_005468.1:p.Thr1181=
XM_011521148.1:c.2323A= XP_011519450.1:p.Thr775=
XM_011521148.2:c.2323A= XP_011519450.1:p.Thr775=
NM_005477.3:c.3541A= MANE Select NP_005468.1:p.Thr1181=