Canonical Allele Identifier: CA7648794
Gene: HCN4 HGNC NCBI

Linked Data

dbSNP Id: rs758039194
ExAC: 15:73614839 G / T
gnomAD v2: 15-73614839-G-T
gnomAD v4: 15-73322498-G-T
MyVariant Identifiers: chr15:g.73614839G>T (hg19) chr15:g.73322498G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73322498G>T , CM000677.2:g.73322498G>T GRCh38
NC_000015.9:g.73614839G>T , CM000677.1:g.73614839G>T GRCh37
NC_000015.8:g.71401892G>T NCBI36
NG_009063.1:g.51767C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.3595C>A MANE Select ENSP00000261917.3:p.Leu1199Met
ENST00000261917.3:c.3595C>A ENSP00000261917.3:p.Leu1199Met
NM_005477.2:c.3595C>A NP_005468.1:p.Leu1199Met
XM_011521148.1:c.2377C>A XP_011519450.1:p.Leu793Met
XM_011521148.2:c.2377C>A XP_011519450.1:p.Leu793Met
NM_005477.3:c.3595C>A MANE Select NP_005468.1:p.Leu1199Met
Search 100 bp 5'
Search 100 bp 3'