Canonical Allele Identifier: CA393098632
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2897971
ClinVar RCV Id: RCV003615257
MyVariant Identifiers: chr15:g.73660377C>G (hg19) chr15:g.73368036C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368036C>G , CM000677.2:g.73368036C>G GRCh38
NC_000015.9:g.73660377C>G , CM000677.1:g.73660377C>G GRCh37
NC_000015.8:g.71447430C>G NCBI36
NG_009063.1:g.6229G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.235G>C MANE Select ENSP00000261917.3:p.Gly79Arg
ENST00000261917.3:c.235G>C ENSP00000261917.3:p.Gly79Arg
NM_005477.2:c.235G>C NP_005468.1:p.Gly79Arg
NM_005477.3:c.235G>C MANE Select NP_005468.1:p.Gly79Arg
Search 100 bp 5'
Search 100 bp 3'