Canonical Allele Identifier: CA2187169586
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73332029C= , CM000677.2:g.73332029C= GRCh38
NC_000015.9:g.73624370C= , CM000677.1:g.73624370C= GRCh37
NC_000015.8:g.71411423C= NCBI36
NG_009063.1:g.42236G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1371+102G= MANE Select ENSP00000261917.3:n.1371+102G=
ENST00000261917.3:c.1371+102G= ENSP00000261917.3:n.1371+102G=
NM_005477.2:c.1371+102G= NP_005468.1:n.1371+102G=
XM_011521148.1:c.153+102G= XP_011519450.1:n.153+102G=
XM_011521148.2:c.153+102G= XP_011519450.1:n.153+102G=
NM_005477.3:c.1371+102G= MANE Select NP_005468.1:n.1371+102G=