Canonical Allele Identifier: CA2187167414
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329600G= , CM000677.2:g.73329600G= GRCh38
NC_000015.9:g.73621941G= , CM000677.1:g.73621941G= GRCh37
NC_000015.8:g.71408994G= NCBI36
NG_009063.1:g.44665C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1563C= MANE Select ENSP00000261917.3:p.Asp521=
ENST00000261917.3:c.1563C= ENSP00000261917.3:p.Asp521=
NM_005477.2:c.1563C= NP_005468.1:p.Asp521=
XM_011521148.1:c.345C= XP_011519450.1:p.Asp115=
XM_011521148.2:c.345C= XP_011519450.1:p.Asp115=
NM_005477.3:c.1563C= MANE Select NP_005468.1:p.Asp521=