Canonical Allele Identifier: CA393089956
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2823404
ClinVar RCV Id: RCV003613811
MyVariant Identifiers: chr15:g.73616466A>G (hg19) chr15:g.73324125A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73324125A>G , CM000677.2:g.73324125A>G GRCh38
NC_000015.9:g.73616466A>G , CM000677.1:g.73616466A>G GRCh37
NC_000015.8:g.71403519A>G NCBI36
NG_009063.1:g.50140T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2107T>C MANE Select ENSP00000261917.3:p.Phe703Leu
ENST00000261917.3:c.2107T>C ENSP00000261917.3:p.Phe703Leu
NM_005477.2:c.2107T>C NP_005468.1:p.Phe703Leu
XM_011521148.1:c.889T>C XP_011519450.1:p.Phe297Leu
XM_011521148.2:c.889T>C XP_011519450.1:p.Phe297Leu
NM_005477.3:c.2107T>C MANE Select NP_005468.1:p.Phe703Leu
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