Canonical Allele Identifier: CA393097190
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73659911A>C (hg19) chr15:g.73367570A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367570A>C , CM000677.2:g.73367570A>C GRCh38
NC_000015.9:g.73659911A>C , CM000677.1:g.73659911A>C GRCh37
NC_000015.8:g.71446964A>C NCBI36
NG_009063.1:g.6695T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.701T>G MANE Select ENSP00000261917.3:p.Phe234Cys
ENST00000261917.3:c.701T>G ENSP00000261917.3:p.Phe234Cys
NM_005477.2:c.701T>G NP_005468.1:p.Phe234Cys
NM_005477.3:c.701T>G MANE Select NP_005468.1:p.Phe234Cys
Search 100 bp 5'
Search 100 bp 3'