Canonical Allele Identifier: CA491479905
Gene: HCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 1143095
ClinVar RCV Id: RCV001481129
dbSNP Id: rs2151228694
gnomAD v4: 15-73368100-G-T
MyVariant Identifiers: chr15:g.73660441G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.73368100G>T , CM000677.2:g.73368100G>T GRCh38
NC_000015.9:g.73660441G>T , CM000677.1:g.73660441G>T GRCh37
NC_000015.8:g.71447494G>T NCBI36
NG_009063.1:g.6165C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000261917.4:c.171C>A MANE Select ENSP00000261917.3:p.Ser57=
ENST00000261917.3:c.171C>A ENSP00000261917.3:p.Ser57=
NM_005477.2:c.171C>A NP_005468.1:p.Ser57=
NM_005477.3:c.171C>A MANE Select NP_005468.1:p.Ser57=
Search 100 bp 5'
Search 100 bp 3'