Canonical Allele Identifier: CA393098756
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2110322
ClinVar RCV Id: RCV003042297
gnomAD v4: 15-73368080-C-T
MyVariant Identifiers: chr15:g.73660421C>T (hg19) chr15:g.73368080C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368080C>T , CM000677.2:g.73368080C>T GRCh38
NC_000015.9:g.73660421C>T , CM000677.1:g.73660421C>T GRCh37
NC_000015.8:g.71447474C>T NCBI36
NG_009063.1:g.6185G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000261917.4:c.191G>A MANE Select ENSP00000261917.3:p.Gly64Asp
ENST00000261917.3:c.191G>A ENSP00000261917.3:p.Gly64Asp
NM_005477.2:c.191G>A NP_005468.1:p.Gly64Asp
NM_005477.3:c.191G>A MANE Select NP_005468.1:p.Gly64Asp
Search 100 bp 5'
Search 100 bp 3'