Canonical Allele Identifier: CA2187194585
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367856G= , CM000677.2:g.73367856G= GRCh38
NC_000015.9:g.73660197G= , CM000677.1:g.73660197G= GRCh37
NC_000015.8:g.71447250G= NCBI36
NG_009063.1:g.6409C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.415C= MANE Select ENSP00000261917.3:p.Pro139=
ENST00000261917.3:c.415C= ENSP00000261917.3:p.Pro139=
NM_005477.2:c.415C= NP_005468.1:p.Pro139=
NM_005477.3:c.415C= MANE Select NP_005468.1:p.Pro139=