Canonical Allele Identifier: CA393089451
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73616234A>T (hg19) chr15:g.73323893A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323893A>T , CM000677.2:g.73323893A>T GRCh38
NC_000015.9:g.73616234A>T , CM000677.1:g.73616234A>T GRCh37
NC_000015.8:g.71403287A>T NCBI36
NG_009063.1:g.50372T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2200T>A MANE Select ENSP00000261917.3:p.Phe734Ile
ENST00000261917.3:c.2200T>A ENSP00000261917.3:p.Phe734Ile
NM_005477.2:c.2200T>A NP_005468.1:p.Phe734Ile
XM_011521148.1:c.982T>A XP_011519450.1:p.Phe328Ile
XM_011521148.2:c.982T>A XP_011519450.1:p.Phe328Ile
NM_005477.3:c.2200T>A MANE Select NP_005468.1:p.Phe734Ile
Search 100 bp 5'
Search 100 bp 3'