Canonical Allele Identifier: CA2187169592
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332036G= , CM000677.2:g.73332036G= GRCh38
NC_000015.9:g.73624377G= , CM000677.1:g.73624377G= GRCh37
NC_000015.8:g.71411430G= NCBI36
NG_009063.1:g.42229C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1371+95C= MANE Select ENSP00000261917.3:n.1371+95C=
ENST00000261917.3:c.1371+95C= ENSP00000261917.3:n.1371+95C=
NM_005477.2:c.1371+95C= NP_005468.1:n.1371+95C=
XM_011521148.1:c.153+95C= XP_011519450.1:n.153+95C=
XM_011521148.2:c.153+95C= XP_011519450.1:n.153+95C=
NM_005477.3:c.1371+95C= MANE Select NP_005468.1:n.1371+95C=