Canonical Allele Identifier: CA491479645
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2743097
ClinVar RCV Id: RCV003504585
dbSNP Id: rs956956393
gnomAD v4: 15-73367806-G-T
MyVariant Identifiers: chr15:g.73660147G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73367806G>T , CM000677.2:g.73367806G>T GRCh38
NC_000015.9:g.73660147G>T , CM000677.1:g.73660147G>T GRCh37
NC_000015.8:g.71447200G>T NCBI36
NG_009063.1:g.6459C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.465C>A MANE Select ENSP00000261917.3:p.Pro155=
ENST00000261917.3:c.465C>A ENSP00000261917.3:p.Pro155=
NM_005477.2:c.465C>A NP_005468.1:p.Pro155=
NM_005477.3:c.465C>A MANE Select NP_005468.1:p.Pro155=
Search 100 bp 5'
Search 100 bp 3'