Canonical Allele Identifier: CA2187194539
Gene: HCN4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367757G= , CM000677.2:g.73367757G= GRCh38
NC_000015.9:g.73660098G= , CM000677.1:g.73660098G= GRCh37
NC_000015.8:g.71447151G= NCBI36
NG_009063.1:g.6508C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.514C= MANE Select ENSP00000261917.3:p.Pro172=
ENST00000261917.3:c.514C= ENSP00000261917.3:p.Pro172=
NM_005477.2:c.514C= NP_005468.1:p.Pro172=
NM_005477.3:c.514C= MANE Select NP_005468.1:p.Pro172=
Search 100 bp 5'
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