Canonical Allele Identifier: CA393097105
Gene: HCN4 HGNC NCBI

Linked Data

COSMIC: COSM5506480
MyVariant Identifiers: chr15:g.73659885C>T (hg19) chr15:g.73367544C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367544C>T , CM000677.2:g.73367544C>T GRCh38
NC_000015.9:g.73659885C>T , CM000677.1:g.73659885C>T GRCh37
NC_000015.8:g.71446938C>T NCBI36
NG_009063.1:g.6721G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.727G>A MANE Select ENSP00000261917.3:p.Glu243Lys
ENST00000261917.3:c.727G>A ENSP00000261917.3:p.Glu243Lys
NM_005477.2:c.727G>A NP_005468.1:p.Glu243Lys
NM_005477.3:c.727G>A MANE Select NP_005468.1:p.Glu243Lys
Search 100 bp 5'
Search 100 bp 3'