Canonical Allele Identifier: CA393085488
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73615077G>T (hg19) chr15:g.73322736G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322736G>T , CM000677.2:g.73322736G>T GRCh38
NC_000015.9:g.73615077G>T , CM000677.1:g.73615077G>T GRCh37
NC_000015.8:g.71402130G>T NCBI36
NG_009063.1:g.51529C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3357C>A MANE Select ENSP00000261917.3:p.Phe1119Leu
ENST00000261917.3:c.3357C>A ENSP00000261917.3:p.Phe1119Leu
NM_005477.2:c.3357C>A NP_005468.1:p.Phe1119Leu
XM_011521148.1:c.2139C>A XP_011519450.1:p.Phe713Leu
XM_011521148.2:c.2139C>A XP_011519450.1:p.Phe713Leu
NM_005477.3:c.3357C>A MANE Select NP_005468.1:p.Phe1119Leu
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