Canonical Allele Identifier: CA2187167352
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329554G= , CM000677.2:g.73329554G= GRCh38
NC_000015.9:g.73621895G= , CM000677.1:g.73621895G= GRCh37
NC_000015.8:g.71408948G= NCBI36
NG_009063.1:g.44711C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1590+19C= MANE Select ENSP00000261917.3:n.1590+19C=
ENST00000261917.3:c.1590+19C= ENSP00000261917.3:n.1590+19C=
NM_005477.2:c.1590+19C= NP_005468.1:n.1590+19C=
XM_011521148.1:c.372+19C= XP_011519450.1:n.372+19C=
XM_011521148.2:c.372+19C= XP_011519450.1:n.372+19C=
NM_005477.3:c.1590+19C= MANE Select NP_005468.1:n.1590+19C=