Canonical Allele Identifier: CA2187194630
Gene: HCN4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367937C= , CM000677.2:g.73367937C= GRCh38
NC_000015.9:g.73660278C= , CM000677.1:g.73660278C= GRCh37
NC_000015.8:g.71447331C= NCBI36
NG_009063.1:g.6328G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.334G= MANE Select ENSP00000261917.3:p.Gly112=
ENST00000261917.3:c.334G= ENSP00000261917.3:p.Gly112=
NM_005477.2:c.334G= NP_005468.1:p.Gly112=
NM_005477.3:c.334G= MANE Select NP_005468.1:p.Gly112=