Canonical Allele Identifier: CA393093613
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73621979A>T (hg19) chr15:g.73329638A>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73329638A>T , CM000677.2:g.73329638A>T GRCh38
NC_000015.9:g.73621979A>T , CM000677.1:g.73621979A>T GRCh37
NC_000015.8:g.71409032A>T NCBI36
NG_009063.1:g.44627T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.1525T>A MANE Select ENSP00000261917.3:p.Phe509Ile
ENST00000261917.3:c.1525T>A ENSP00000261917.3:p.Phe509Ile
NM_005477.2:c.1525T>A NP_005468.1:p.Phe509Ile
XM_011521148.1:c.307T>A XP_011519450.1:p.Phe103Ile
XM_011521148.2:c.307T>A XP_011519450.1:p.Phe103Ile
NM_005477.3:c.1525T>A MANE Select NP_005468.1:p.Phe509Ile
Search 100 bp 5'
Search 100 bp 3'