Canonical Allele Identifier: CA393088995
Gene: HCN4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr15:g.73616050A>C (hg19) chr15:g.73323709A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73323709A>C , CM000677.2:g.73323709A>C GRCh38
NC_000015.9:g.73616050A>C , CM000677.1:g.73616050A>C GRCh37
NC_000015.8:g.71403103A>C NCBI36
NG_009063.1:g.50556T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.2384T>G MANE Select ENSP00000261917.3:p.Leu795Arg
ENST00000261917.3:c.2384T>G ENSP00000261917.3:p.Leu795Arg
NM_005477.2:c.2384T>G NP_005468.1:p.Leu795Arg
XM_011521148.1:c.1166T>G XP_011519450.1:p.Leu389Arg
XM_011521148.2:c.1166T>G XP_011519450.1:p.Leu389Arg
NM_005477.3:c.2384T>G MANE Select NP_005468.1:p.Leu795Arg
Search 100 bp 5'
Search 100 bp 3'