Canonical Allele Identifier: CA393099283
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1392598
ClinVar RCV Id: RCV001882222
dbSNP Id: rs1267513363
gnomAD v2: 15-73660604-T-C
gnomAD v3: 15-73368263-T-C
gnomAD v4: 15-73368263-T-C
MyVariant Identifiers: chr15:g.73660604T>C (hg19) chr15:g.73368263T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368263T>C , CM000677.2:g.73368263T>C GRCh38
NC_000015.9:g.73660604T>C , CM000677.1:g.73660604T>C GRCh37
NC_000015.8:g.71447657T>C NCBI36
NG_009063.1:g.6002A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.8A>G MANE Select ENSP00000261917.3:p.Lys3Arg
ENST00000261917.3:c.8A>G ENSP00000261917.3:p.Lys3Arg
NM_005477.2:c.8A>G NP_005468.1:p.Lys3Arg
NM_005477.3:c.8A>G MANE Select NP_005468.1:p.Lys3Arg
Search 100 bp 5'
Search 100 bp 3'