Canonical Allele Identifier: CA2187186448
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322686C= , CM000677.2:g.73322686C= GRCh38
NC_000015.9:g.73615027C= , CM000677.1:g.73615027C= GRCh37
NC_000015.8:g.71402080C= NCBI36
NG_009063.1:g.51579G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.3407G= MANE Select ENSP00000261917.3:p.Gly1136=
ENST00000261917.3:c.3407G= ENSP00000261917.3:p.Gly1136=
NM_005477.2:c.3407G= NP_005468.1:p.Gly1136=
XM_011521148.1:c.2189G= XP_011519450.1:p.Gly730=
XM_011521148.2:c.2189G= XP_011519450.1:p.Gly730=
NM_005477.3:c.3407G= MANE Select NP_005468.1:p.Gly1136=