Canonical Allele Identifier: CA2187194780
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368220C= , CM000677.2:g.73368220C= GRCh38
NC_000015.9:g.73660561C= , CM000677.1:g.73660561C= GRCh37
NC_000015.8:g.71447614C= NCBI36
NG_009063.1:g.6045G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.51G= MANE Select ENSP00000261917.3:p.Gln17=
ENST00000261917.3:c.51G= ENSP00000261917.3:p.Gln17=
NM_005477.2:c.51G= NP_005468.1:p.Gln17=
NM_005477.3:c.51G= MANE Select NP_005468.1:p.Gln17=
Search 100 bp 5'
Search 100 bp 3'