Canonical Allele Identifier: CA491479567
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1153371
ClinVar RCV Id: RCV001495024 RCV004037347
dbSNP Id: rs2151228480
gnomAD v4: 15-73367740-G-A
MyVariant Identifiers: chr15:g.73660081G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367740G>A , CM000677.2:g.73367740G>A GRCh38
NC_000015.9:g.73660081G>A , CM000677.1:g.73660081G>A GRCh37
NC_000015.8:g.71447134G>A NCBI36
NG_009063.1:g.6525C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.531C>T MANE Select ENSP00000261917.3:p.Ala177=
ENST00000261917.3:c.531C>T ENSP00000261917.3:p.Ala177=
NM_005477.2:c.531C>T NP_005468.1:p.Ala177=
NM_005477.3:c.531C>T MANE Select NP_005468.1:p.Ala177=
Search 100 bp 5'
Search 100 bp 3'