Canonical Allele Identifier: CA7649442
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1044695
ClinVar RCV Id: RCV001348975
dbSNP Id: rs371771170
ExAC: 15:73659951 T / C
gnomAD v2: 15-73659951-T-C
gnomAD v3: 15-73367610-T-C
gnomAD v4: 15-73367610-T-C
MyVariant Identifiers: chr15:g.73659951T>C (hg19) chr15:g.73367610T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367610T>C , CM000677.2:g.73367610T>C GRCh38
NC_000015.9:g.73659951T>C , CM000677.1:g.73659951T>C GRCh37
NC_000015.8:g.71447004T>C NCBI36
NG_009063.1:g.6655A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.661A>G MANE Select ENSP00000261917.3:p.Met221Val
ENST00000261917.3:c.661A>G ENSP00000261917.3:p.Met221Val
NM_005477.2:c.661A>G NP_005468.1:p.Met221Val
NM_005477.3:c.661A>G MANE Select NP_005468.1:p.Met221Val
Search 100 bp 5'
Search 100 bp 3'