Canonical Allele Identifier: CA393093604
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73621977G>T (hg19) chr15:g.73329636G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329636G>T , CM000677.2:g.73329636G>T GRCh38
NC_000015.9:g.73621977G>T , CM000677.1:g.73621977G>T GRCh37
NC_000015.8:g.71409030G>T NCBI36
NG_009063.1:g.44629C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.1527C>A MANE Select ENSP00000261917.3:p.Phe509Leu
ENST00000261917.3:c.1527C>A ENSP00000261917.3:p.Phe509Leu
NM_005477.2:c.1527C>A NP_005468.1:p.Phe509Leu
XM_011521148.1:c.309C>A XP_011519450.1:p.Phe103Leu
XM_011521148.2:c.309C>A XP_011519450.1:p.Phe103Leu
NM_005477.3:c.1527C>A MANE Select NP_005468.1:p.Phe509Leu
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