Canonical Allele Identifier: CA2187188654
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323789G= , CM000677.2:g.73323789G= GRCh38
NC_000015.9:g.73616130G= , CM000677.1:g.73616130G= GRCh37
NC_000015.8:g.71403183G= NCBI36
NG_009063.1:g.50476C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2304C= MANE Select ENSP00000261917.3:p.Thr768=
ENST00000261917.3:c.2304C= ENSP00000261917.3:p.Thr768=
NM_005477.2:c.2304C= NP_005468.1:p.Thr768=
XM_011521148.1:c.1086C= XP_011519450.1:p.Thr362=
XM_011521148.2:c.1086C= XP_011519450.1:p.Thr362=
NM_005477.3:c.2304C= MANE Select NP_005468.1:p.Thr768=